A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15192566



Internal ID6564045
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635936
Supporting Variants
SamplesNA20757
Known GenesATP10A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15192566
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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