A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15552013



Internal ID6802070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85322996..85326267hg38UCSC Ensembl
Innerchr16:85322996..85326267hg38UCSC Ensembl
Outerchr16:85322766..85326431hg38UCSC Ensembl
chr16:85356602..85359873hg19UCSC Ensembl
Innerchr16:85356602..85359873hg19UCSC Ensembl
Outerchr16:85356372..85360037hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg383272
hg193272
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639462
Supporting Variants
SamplesNA20890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15552013
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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