A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638788



Internal ID7025573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61995841..62000441hg38UCSC Ensembl
Innerchr16:61995841..62000441hg38UCSC Ensembl
Outerchr16:61995685..62000635hg38UCSC Ensembl
chr16:62029745..62034345hg19UCSC Ensembl
Innerchr16:62029745..62034345hg19UCSC Ensembl
Outerchr16:62029589..62034539hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg384601
hg194601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15496303, essv15496304
SamplesHG03862, HG02787
Known GenesCDH8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638788
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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