A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1475n54



Internal ID18993651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133257500..133333210hg38UCSC Ensembl
chr10:135071004..135146714hg19UCSC Ensembl
chr10:134920995..134996704hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3875711
hg1975711
hg1875710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552588, nsv552591
SamplesHGDP01251, 1780862540_A, HGDP00784, HGDP00974
Known GenesADAM8, CALY, TUBGCP2, ZNF511
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1475n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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