A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637673



Internal ID6677775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3653616..3669650hg38UCSC Ensembl
Innerchr16:3653616..3669650hg38UCSC Ensembl
Outerchr16:3653437..3669840hg38UCSC Ensembl
chr16:3703617..3719651hg19UCSC Ensembl
Innerchr16:3703617..3719651hg19UCSC Ensembl
Outerchr16:3703438..3719841hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3816035
hg1916035
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15363262, essv15363263
SamplesHG00734, HG01606
Known GenesDNASE1, TRAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637673
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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