A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701001



Internal ID15437653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164884778..164884988hg38UCSC Ensembl
Innerchr6:165298267..165298477hg19UCSC Ensembl
Innerchr6:165218257..165218467hg18UCSC Ensembl
Innerchr6:165268678..165268888hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38211
hg19211
hg18211
hg17211
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521153
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701001
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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