A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670377



Internal ID15407029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:105204296..105213575hg38UCSC Ensembl
Innerchr6:105652171..105661450hg19UCSC Ensembl
Innerchr6:105758864..105768143hg18UCSC Ensembl
Innerchr6:105758864..105768143hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg389280
hg199280
hg189280
hg179280
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516715
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670377
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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