A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15190613



Internal ID6836393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25686288..25687237hg38UCSC Ensembl
Innerchr15:25686288..25687237hg38UCSC Ensembl
Outerchr15:25685947..25687639hg38UCSC Ensembl
chr15:25931435..25932384hg19UCSC Ensembl
Innerchr15:25931435..25932384hg19UCSC Ensembl
Outerchr15:25931094..25932786hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38950
hg19950
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635933
Supporting Variants
SamplesNA20905
Known GenesATP10A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15190613
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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