A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1466n54



Internal ID22769361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133111093..133112019hg38UCSC Ensembl
chr10:134924597..134925523hg19UCSC Ensembl
chr10:134774587..134775513hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38927
hg19927
hg18927
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552542, nsv552552, nsv552560, nsv552547, nsv552553
Samples
Known GenesGPR123
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1466n54
Frequency
Sample Size17421
Observed Gain53
Observed Loss13
Observed Complex0
Frequencyn/a


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