A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581650



Internal ID16022373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:43225469..43227728hg38UCSC Ensembl
Innerchr2:43452608..43454867hg19UCSC Ensembl
Innerchr2:43306112..43308371hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg382260
hg192260
hg182260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6827n54
Supporting Variantsnssv907887
Samples
Known GenesLINC01126, ZFP36L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581650
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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