A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3868n54



Internal ID22771763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97337382..97337965hg38UCSC Ensembl
chr14:97803719..97804302hg19UCSC Ensembl
chr14:96873472..96874055hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38584
hg19584
hg18584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565655, nsv565656
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3868n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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