A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3956n54



Internal ID20137380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104706874..104719230hg38UCSC Ensembl
chr14:105173211..105185567hg19UCSC Ensembl
chr14:104244256..104256612hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3812357
hg1912357
hg1812357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566067, nsv566068
Samples
Known GenesINF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3956n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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