A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581197



Internal ID16368606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:24491300..24492157hg38UCSC Ensembl
Innerchr2:24714169..24715026hg19UCSC Ensembl
Innerchr2:24567673..24568530hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38858
hg19858
hg18858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6736n54
Supporting Variantsnssv904507
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581197
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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