A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635936



Internal ID7022733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25737793..25747258hg38UCSC Ensembl
chr15:25982940..25992405hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg389466
hg199466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15192566, essv15192569, essv15192567, essv15192568
SamplesNA20874, NA20757, NA21122, NA21126
Known GenesATP10A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635936
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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