A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15192013



Internal ID5118131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25686657..25686875hg38UCSC Ensembl
Innerchr15:25686662..25686870hg38UCSC Ensembl
Outerchr15:25686652..25686880hg38UCSC Ensembl
chr15:25931804..25932022hg19UCSC Ensembl
Innerchr15:25931809..25932017hg19UCSC Ensembl
Outerchr15:25931799..25932027hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635934
Supporting Variants
SamplesNA18562
Known GenesATP10A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15192013
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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