A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581196



Internal ID16368605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:24491300..24491935hg38UCSC Ensembl
Innerchr2:24714169..24714804hg19UCSC Ensembl
Innerchr2:24567673..24568308hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38636
hg19636
hg18636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6736n54
Supporting Variantsnssv904506
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581196
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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