A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1001n54



Internal ID22768896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20573498..20640390hg38UCSC Ensembl
chr10:20862427..20929319hg19UCSC Ensembl
chr10:20902433..20969325hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3866893
hg1966893
hg1866893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550199, nsv550198
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1001n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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