A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581771



Internal ID16022494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:47638994..47729705hg38UCSC Ensembl
Innerchr2:47866133..47956844hg19UCSC Ensembl
Innerchr2:47719637..47810348hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3890712
hg1990712
hg1890712
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150444
SamplesHGDP00210
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581771
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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