A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613952



Internal ID16401361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27845762..27897126hg38UCSC Ensembl
Innerchr9:27845760..27897124hg19UCSC Ensembl
Innerchr9:27835760..27887124hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3851365
hg1951365
hg1851365
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12621n54
Supporting Variantsnssv1156753
SamplesHGDP00843
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613952
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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