A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581201



Internal ID16368610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:24919602..24920754hg38UCSC Ensembl
Innerchr2:25142471..25143623hg19UCSC Ensembl
Innerchr2:24995975..24997127hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg381153
hg191153
hg181153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv904511
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581201
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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