A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv963n54



Internal ID20134387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14945441..15018277hg38UCSC Ensembl
chr10:14987440..15060276hg19UCSC Ensembl
chr10:15027446..15100282hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3872837
hg1972837
hg1872837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550003, nsv550006
Samples
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv963n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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