A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv904414



Internal ID16198370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:19787679..19895929hg38UCSC Ensembl
Innerchr2:19987440..20095690hg19UCSC Ensembl
Innerchr2:19850921..19959171hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38108251
hg19108251
hg18108251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581155
Supporting Variants
Samples
Known GenesLINC00954
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv904414
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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