A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581115



Internal ID16368524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:18302778..18354614hg38UCSC Ensembl
Innerchr2:18484044..18535880hg19UCSC Ensembl
Innerchr2:18347525..18399361hg18UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3851837
hg1951837
hg1851837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv904170
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581115
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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