A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637588



Internal ID7024379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:799071..846677hg38UCSC Ensembl
Innerchr16:799112..846637hg38UCSC Ensembl
Outerchr16:799031..846718hg38UCSC Ensembl
chr16:849071..896677hg19UCSC Ensembl
Innerchr16:849112..896637hg19UCSC Ensembl
Outerchr16:849031..896718hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3847607
hg1947607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15355403
SamplesHG00759
Known GenesGNG13, PRR25
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637588
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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