A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581236



Internal ID16021959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:25673076..25674021hg38UCSC Ensembl
Innerchr2:25895945..25896890hg19UCSC Ensembl
Innerchr2:25749449..25750394hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38946
hg19946
hg18946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6742n54
Supporting Variantsnssv904587, nssv904588
Samples
Known GenesDTNB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581236
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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