A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15191957



Internal ID4945747
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
SamplesNA12813
Known GenesATP10A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15191957
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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