A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696895



Internal ID15433547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:11938439..11942138hg38UCSC Ensembl
Innerchr6:11938672..11942371hg19UCSC Ensembl
Innerchr6:12046658..12050357hg18UCSC Ensembl
Innerchr6:12046658..12050357hg17UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg383700
hg193700
hg183700
hg173700
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519516
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696895
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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