A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665528



Internal ID15055494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7149893..7511473hg38UCSC Ensembl
Innerchr8:7007415..7368995hg19UCSC Ensembl
Innerchr8:6994825..7356405hg18UCSC Ensembl
Innerchr8:6994825..7356405hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38361581
hg19361581
hg18361581
hg17361581
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515968
Supporting Variants
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB109P1B, DEFB4B, FAM66B, LINC00965, SPAG11B, USP17L1P, USP17L4, ZNF705G
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665528
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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