A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696646



Internal ID15433298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:8986249..9137048hg38UCSC Ensembl
Innerchr6:8986482..9137281hg19UCSC Ensembl
Innerchr6:8931481..9082280hg18UCSC Ensembl
Innerchr6:8931481..9082280hg17UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38150800
hg19150800
hg18150800
hg17150800
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519164
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696646
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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