A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3598n54



Internal ID22771493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27989467..28049942hg38UCSC Ensembl
chr14:28458673..28519148hg19UCSC Ensembl
chr14:27528513..27589002hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3860476
hg1960476
hg1860490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564145, nsv564148
SamplesHGDP00630
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3598n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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