A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv935n54



Internal ID20134359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3044294..3125271hg38UCSC Ensembl
chr10:3086486..3167463hg19UCSC Ensembl
chr10:3076486..3157463hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg3880978
hg1980978
hg1880978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv549812, nsv549813, nsv549811
SamplesHGDP01085, HGDP00466, HGDP00465
Known GenesPFKP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv935n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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