A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698336



Internal ID15434988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140554890..140647155hg38UCSC Ensembl
Innerchr6:140876027..140968292hg19UCSC Ensembl
Innerchr6:140917720..141009985hg18UCSC Ensembl
Innerchr6:140917720..141009985hg17UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3892266
hg1992266
hg1892266
hg1792266
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521710
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698336
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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