A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1212n54



Internal ID22769107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:65012286..65372541hg38UCSC Ensembl
chr10:66772044..67132299hg19UCSC Ensembl
chr10:66442050..66802305hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38360256
hg19360256
hg18360256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551235, nsv551232, nsv551233
SamplesHGDP00145, HGDP00076, HGDP00155
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1212n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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