A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697108



Internal ID15087074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:156751681..156788667hg38UCSC Ensembl
Innerchr6:157072815..157109801hg19UCSC Ensembl
Innerchr6:157114507..157151493hg18UCSC Ensembl
Innerchr6:157164928..157201914hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3836987
hg1936987
hg1836987
hg1736987
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519889
Supporting Variants
Samples
Known GenesARID1B, MIR4466
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697108
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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