A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15499291



Internal ID5763339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64611581..64618228hg38UCSC Ensembl
Innerchr16:64611581..64618228hg38UCSC Ensembl
Outerchr16:64611081..64618728hg38UCSC Ensembl
chr16:64645484..64652131hg19UCSC Ensembl
Innerchr16:64645484..64652131hg19UCSC Ensembl
Outerchr16:64644984..64652631hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg386648
hg196648
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638837
Supporting Variants
SamplesNA19131
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15499291
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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