A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581407



Internal ID16368816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35616801..35852274hg38UCSC Ensembl
Innerchr2:35841867..36077340hg19UCSC Ensembl
Innerchr2:35695371..35930844hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38235474
hg19235474
hg18235474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6771n54
Supporting Variantsnssv906225
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581407
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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