A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581008



Internal ID16368417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13051151..13142111hg38UCSC Ensembl
Innerchr2:13191276..13282236hg19UCSC Ensembl
Innerchr2:13108727..13199687hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3890961
hg1990961
hg1890961
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6700n54
Supporting Variantsnssv1150394
Samples1788485588_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581008
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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