A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694635



Internal ID15084601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149761534..149885817hg38UCSC Ensembl
Innerchr7:149458623..149582906hg19UCSC Ensembl
Innerchr7:149089556..149213839hg18UCSC Ensembl
Innerchr7:148896271..149020554hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38124284
hg19124284
hg18124284
hg17124284
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521861
Supporting Variants
Samples
Known GenesATP6V0E2, ATP6V0E2-AS1, SSPO, ZNF467, ZNF862
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694635
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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