A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3871n54



Internal ID22771766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98710831..98727250hg38UCSC Ensembl
chr14:99177168..99193587hg19UCSC Ensembl
chr14:98246921..98263340hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3816420
hg1916420
hg1816420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565669, nsv565668
Samples
Known GenesC14orf177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3871n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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