I obviously don't know why you want to visualise your gVCF files, but I would think you need to do further processing (variant calling: GATK GenotypeGVCFs) to make the results meaningful.
IGV works with GVCF files. The only caveat is that you have to use a ".g.vcf" extension rather than a ".vcf" extension (or ".g.vcf.gz" rather than ".vcf.gz").
Re "why you want to visualise your gVCF files": I think it's a good idea to visualise intermediate results as a sanity check. For example, if my data came from exome sequencing, then I would expect IGV to show gVCF records concentrated in exonic regions.
I obviously don't know why you want to visualise your gVCF files, but I would think you need to do further processing (variant calling: GATK GenotypeGVCFs) to make the results meaningful.
duplicate of Best visual and interactive genotype matrix (VCF) exploration tool
Thanks for this comment. The post you are referring to is about VCF files, does all the same applies to files in gVCF format?
as far as I know gvcf ( https://sites.google.com/site/gvcftools/home/about-gvcf / https://software.broadinstitute.org/gatk/guide/article?id=4017 ) are VCF.
i think gvcfs are the likelihood of variants so that we can do joint genotyping, and variant calling