A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6951n54



Internal ID22774846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:89887267..90276638hg38UCSC Ensembl
chr2:89926077..90315498hg19UCSC Ensembl
chr2:89563119..89952803hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38389372
hg19389422
hg18389685
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv582400, nsv582403, nsv582402, nsv582401
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6951n54
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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