A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700466



Internal ID15437118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170130646..170137323hg38UCSC Ensembl
Innerchr6:170445870..170452547hg19UCSC Ensembl
Innerchr6:170287795..170294472hg18UCSC Ensembl
Innerchr6:170363502..170370179hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg386678
hg196678
hg186678
hg176678
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524520
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700466
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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