A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581655



Internal ID16369064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:43264911..43326810hg38UCSC Ensembl
Innerchr2:43492050..43553949hg19UCSC Ensembl
Innerchr2:43345554..43407453hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3861900
hg1961900
hg1861900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6829n54
Supporting Variantsnssv907891
Samples
Known GenesTHADA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581655
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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