A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3701n54



Internal ID22771596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:46833016..46926598hg38UCSC Ensembl
chr14:47302219..47395801hg19UCSC Ensembl
chr14:46371969..46465551hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3893583
hg1993583
hg1893583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564758, nsv564761, nsv564759, nsv564760
Samples
Known GenesMDGA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3701n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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