A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581234



Internal ID16021957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:25673076..25673834hg38UCSC Ensembl
Innerchr2:25895945..25896703hg19UCSC Ensembl
Innerchr2:25749449..25750207hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38759
hg19759
hg18759
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv904583, nssv904584, nssv904585
Samples
Known GenesDTNB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581234
Frequency
Sample Size17421
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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