A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693390



Internal ID15430042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:68525208..68532128hg38UCSC Ensembl
Innerchr6:69235100..69242020hg19UCSC Ensembl
Innerchr6:69291821..69298741hg18UCSC Ensembl
Innerchr6:69291821..69298741hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg386921
hg196921
hg186921
hg176921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515885
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693390
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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