A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4500n54



Internal ID20137924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42908911..43153107hg38UCSC Ensembl
chr15:43201109..43445305hg19UCSC Ensembl
chr15:40988401..41232597hg18UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38244197
hg19244197
hg18244197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569240, nsv569239, nsv569242
Samples
Known GenesTMEM62, TTBK2, UBR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4500n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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