A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696279



Internal ID15086245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9699362..9757728hg38UCSC Ensembl
Innerchr19:9810038..9868404hg19UCSC Ensembl
Innerchr19:9671038..9729404hg18UCSC Ensembl
Innerchr19:9671038..9729404hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3858367
hg1958367
hg1858367
hg1758367
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518826
Supporting Variants
Samples
Known GenesZNF812, ZNF846
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696279
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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