A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701466



Internal ID15091432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26313120..26322757hg38UCSC Ensembl
Innerchr6:26313348..26322985hg19UCSC Ensembl
Innerchr6:26421327..26430964hg18UCSC Ensembl
Innerchr6:26421327..26430964hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg389638
hg199638
hg189638
hg179638
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525347
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701466
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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