A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1132014



Internal ID15985200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24650089..24731625hg38UCSC Ensembl
Innerchr9:24650087..24731623hg19UCSC Ensembl
Innerchr9:24640087..24721623hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3881537
hg1981537
hg1881537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613884
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1132014
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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