A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613916



Internal ID16401325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25610274..25643335hg38UCSC Ensembl
Innerchr9:25610272..25643333hg19UCSC Ensembl
Innerchr9:25600272..25633333hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3833062
hg1933062
hg1833062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156739
SamplesHGDP00647
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613916
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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