A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696288



Internal ID15432940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:139448930..139479755hg38UCSC Ensembl
Innerchr6:139770067..139800892hg19UCSC Ensembl
Innerchr6:139811760..139842585hg18UCSC Ensembl
Innerchr6:139811760..139842585hg17UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3830826
hg1930826
hg1830826
hg1730826
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518835
Supporting Variants
Samples
Known GenesLOC645434
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696288
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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