A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639385



Internal ID6679479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83196037..83201625hg38UCSC Ensembl
Innerchr16:83196037..83201625hg38UCSC Ensembl
Outerchr16:83195689..83202017hg38UCSC Ensembl
chr16:83229642..83235230hg19UCSC Ensembl
Innerchr16:83229642..83235230hg19UCSC Ensembl
Outerchr16:83229294..83235622hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg385589
hg195589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15545326
SamplesHG01510
Known GenesCDH13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639385
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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