A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3870n54



Internal ID22771765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98703893..98735869hg38UCSC Ensembl
chr14:99170230..99202206hg19UCSC Ensembl
chr14:98239983..98271959hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3831977
hg1931977
hg1831977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565667, nsv565666
SamplesHGDP01169
Known GenesC14orf177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3870n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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