A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581256



Internal ID16368665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:29593934..29647339hg38UCSC Ensembl
Innerchr2:29816800..29870205hg19UCSC Ensembl
Innerchr2:29670304..29723709hg18UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg3853406
hg1953406
hg1853406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv904610
Samples
Known GenesALK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581256
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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