A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15316911



Internal ID5503356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88547686..88561271hg38UCSC Ensembl
Innerchr15:88547686..88561271hg38UCSC Ensembl
Outerchr15:88547186..88561771hg38UCSC Ensembl
chr15:89090917..89104502hg19UCSC Ensembl
Innerchr15:89090917..89104502hg19UCSC Ensembl
Outerchr15:89090417..89105002hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3813586
hg1913586
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637173
Supporting Variants
SamplesNA18986
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15316911
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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