A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3702n54



Internal ID22771597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:47011047..47052286hg38UCSC Ensembl
chr14:47480250..47521489hg19UCSC Ensembl
chr14:46550000..46591239hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3841240
hg1941240
hg1841240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564766, nsv564765
Samples
Known GenesMDGA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3702n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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