A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv904589



Internal ID15851859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:25673076..25674072hg38UCSC Ensembl
Innerchr2:25895945..25896941hg19UCSC Ensembl
Innerchr2:25749449..25750445hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38997
hg19997
hg18997
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581237
Supporting Variants
Samples
Known GenesDTNB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv904589
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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