A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613921



Internal ID16401330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25952531..26028354hg38UCSC Ensembl
Innerchr9:25952529..26028352hg19UCSC Ensembl
Innerchr9:25942529..26018352hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3875824
hg1975824
hg1875824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132051
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613921
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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