A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698277



Internal ID15434929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133935822..133941386hg38UCSC Ensembl
Innerchr8:134948065..134953629hg19UCSC Ensembl
Innerchr8:135017247..135022811hg18UCSC Ensembl
Innerchr8:135017247..135022811hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg385565
hg195565
hg185565
hg175565
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521660
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698277
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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