A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639212



Internal ID7025995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78468301..78537680hg38UCSC Ensembl
Innerchr16:78468301..78537680hg38UCSC Ensembl
Outerchr16:78467801..78538180hg38UCSC Ensembl
chr16:78502198..78571577hg19UCSC Ensembl
Innerchr16:78502198..78571577hg19UCSC Ensembl
Outerchr16:78501698..78572077hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3869380
hg1969380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15530142
SamplesNA20814
Known GenesWWOX
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639212
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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