A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6742n54



Internal ID20140166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25673076..25674072hg38UCSC Ensembl
chr2:25895945..25896941hg19UCSC Ensembl
chr2:25749449..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 StatusM
Merged Variants
Supporting Variantsnsv581235, nsv581233, nsv581236, nsv581239, nsv581237
Samples
Known GenesDTNB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6742n54
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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