A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694354



Internal ID15431006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:41651312..41657872hg38UCSC Ensembl
Innerchr6:41619050..41625610hg19UCSC Ensembl
Innerchr6:41727028..41733588hg18UCSC Ensembl
Innerchr6:41727028..41733588hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg386561
hg196561
hg186561
hg176561
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519925
Supporting Variants
Samples
Known GenesMDFI
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694354
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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