A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3950n54



Internal ID22771845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104255189..104335962hg38UCSC Ensembl
chr14:104721526..104802299hg19UCSC Ensembl
chr14:103791279..103873344hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3880774
hg1980774
hg1882066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566039, nsv566037, nsv566038
Samples1782681313_A, 1780862388_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3950n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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