A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3119n54



Internal ID22771014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37491309..37557856hg38UCSC Ensembl
chr13:38065446..38131993hg19UCSC Ensembl
chr13:36963446..37029993hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3866548
hg1966548
hg1866548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv561497, nsv561494, nsv561496, nsv561495
SamplesHGDP00912, HGDP00932
Known GenesLINC00547
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3119n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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