A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519079



Internal ID15099686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33572432..33574761hg38UCSC Ensembl
Innerchr6:33540209..33542538hg19UCSC Ensembl
Innerchr6:33648187..33650516hg18UCSC Ensembl
Innerchr6:33648187..33650516hg17UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg382330
hg192330
hg182330
hg172330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696550
Samples
Known GenesBAK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519079
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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