A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156909



Internal ID15854809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24728498..25294703hg38UCSC Ensembl
Innerchr9:24728496..25294701hg19UCSC Ensembl
Innerchr9:24718496..25284701hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38566206
hg19566206
hg18566206
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613886
Supporting Variants
Samples1780862339_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156909
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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