A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581466



Internal ID16368875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:36126853..36341871hg38UCSC Ensembl
Innerchr2:36353996..36569014hg19UCSC Ensembl
Innerchr2:36207500..36422518hg18UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38215019
hg19215019
hg18215019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6786n54
Supporting Variantsnssv906857
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581466
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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