A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15315953



Internal ID6386982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87088040..87089854hg38UCSC Ensembl
Innerchr15:87088073..87089822hg38UCSC Ensembl
Outerchr15:87088008..87089887hg38UCSC Ensembl
chr15:87631271..87633085hg19UCSC Ensembl
Innerchr15:87631304..87633053hg19UCSC Ensembl
Outerchr15:87631239..87633118hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg381815
hg191815
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637148
Supporting Variants
SamplesNA20332
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15315953
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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