A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698515



Internal ID15435167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:11396370..11472855hg38UCSC Ensembl
Innerchr8:11253879..11330364hg19UCSC Ensembl
Innerchr8:11291289..11367774hg18UCSC Ensembl
Innerchr8:11291289..11367774hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3876486
hg1976486
hg1876486
hg1776486
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522860
Supporting Variants
Samples
Known GenesC8orf12, FAM167A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698515
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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