A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705893



Internal ID15442545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80553271..80588971hg38UCSC Ensembl
Innerchr6:81262988..81298688hg19UCSC Ensembl
Innerchr6:81319707..81355407hg18UCSC Ensembl
Innerchr6:81319707..81355407hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3835701
hg1935701
hg1835701
hg1735701
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522523
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705893
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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