A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1052n54



Internal ID22768947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38576045..38680369hg38UCSC Ensembl
chr10:38869176..38973500hg19UCSC Ensembl
chr10:38909182..39013506hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38104325
hg19104325
hg18104325
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550474, nsv550542, nsv550473
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1052n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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