A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639589



Internal ID6679680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89611865..89614706hg38UCSC Ensembl
Innerchr16:89612015..89614556hg38UCSC Ensembl
Outerchr16:89611715..89614856hg38UCSC Ensembl
chr16:89678273..89681114hg19UCSC Ensembl
Innerchr16:89678423..89680964hg19UCSC Ensembl
Outerchr16:89678123..89681264hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382842
hg192842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15569841
SamplesHG01052
Known GenesDPEP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639589
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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