A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662567



Internal ID15052533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31370751..31372834hg38UCSC Ensembl
Innerchr6:31338528..31340611hg19UCSC Ensembl
Innerchr6:31446507..31448590hg18UCSC Ensembl
Innerchr6:31446507..31448590hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg382084
hg192084
hg182084
hg172084
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517441
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662567
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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