A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639369



Internal ID6679463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82662874..82667635hg38UCSC Ensembl
Innerchr16:82662874..82667635hg38UCSC Ensembl
Outerchr16:82662784..82667832hg38UCSC Ensembl
chr16:82696479..82701240hg19UCSC Ensembl
Innerchr16:82696479..82701240hg19UCSC Ensembl
Outerchr16:82696389..82701437hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg384762
hg194762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15542557, essv15542558
SamplesHG03687, HG04185
Known GenesCDH13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639369
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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