A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3853n54



Internal ID22771748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93987862..93988523hg38UCSC Ensembl
chr14:94454208..94454869hg19UCSC Ensembl
chr14:93523961..93524622hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38662
hg19662
hg18662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565578, nsv565577, nsv565580
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3853n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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