A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4393n54



Internal ID22772288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25686329..25687947hg38UCSC Ensembl
chr15:25931476..25933094hg19UCSC Ensembl
chr15:23482569..23484187hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381619
hg191619
hg181619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568592, nsv568595, nsv568591, nsv568589, nsv568597
Samples
Known GenesATP10A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4393n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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