A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613913



Internal ID16401322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25548321..25621153hg38UCSC Ensembl
Innerchr9:25548319..25621151hg19UCSC Ensembl
Innerchr9:25538319..25611151hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3872833
hg1972833
hg1872833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132048
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613913
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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