A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6929n54



Internal ID22774824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77744657..77812540hg38UCSC Ensembl
chr2:77971783..78039666hg19UCSC Ensembl
chr2:77825291..77893174hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3867884
hg1967884
hg1867884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv582262, nsv582263
SamplesHGDP00491, HGDP00544
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6929n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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