A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638159



Internal ID7024945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20882859..20891671hg38UCSC Ensembl
Innerchr16:20882874..20891656hg38UCSC Ensembl
Outerchr16:20882844..20891686hg38UCSC Ensembl
chr16:20894181..20902993hg19UCSC Ensembl
Innerchr16:20894196..20902978hg19UCSC Ensembl
Outerchr16:20894166..20903008hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg388813
hg198813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15405430
SamplesHG02836
Known GenesDCUN1D3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638159
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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