A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638316



Internal ID7025102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27065722..27087486hg38UCSC Ensembl
Innerchr16:27065769..27087439hg38UCSC Ensembl
Outerchr16:27065675..27087533hg38UCSC Ensembl
chr16:27077043..27098807hg19UCSC Ensembl
Innerchr16:27077090..27098760hg19UCSC Ensembl
Outerchr16:27076996..27098854hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3821765
hg1921765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv500e214
Supporting Variantsessv15439276
SamplesNA18606
Known GenesC16orf82
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638316
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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