A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15188707



Internal ID6212645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25561307..25563713hg38UCSC Ensembl
Innerchr15:25561317..25563703hg38UCSC Ensembl
Outerchr15:25561297..25563723hg38UCSC Ensembl
chr15:25806454..25808860hg19UCSC Ensembl
Innerchr15:25806464..25808850hg19UCSC Ensembl
Outerchr15:25806444..25808870hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg382407
hg192407
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635929
Supporting Variants
SamplesNA19740
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15188707
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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