A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3860n54



Internal ID22771755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93988023..93994487hg38UCSC Ensembl
chr14:94454369..94460833hg19UCSC Ensembl
chr14:93524122..93530586hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg386465
hg196465
hg186465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565593, nsv565608
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3860n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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