A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3693n54



Internal ID22771588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:44701097..44765957hg38UCSC Ensembl
chr14:45170300..45235160hg19UCSC Ensembl
chr14:44240050..44304910hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3864861
hg1964861
hg1864861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564702, nsv564707, nsv564717, nsv564706, nsv564718, nsv564703, nsv564710
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3693n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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