A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892791



Internal ID18836925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10528083..10640166hg38UCSC Ensembl
Outerchr16:10528083..10640166hg38UCSC Ensembl
Innerchr16:10621940..10734023hg19UCSC Ensembl
Outerchr16:10621940..10734023hg19UCSC Ensembl
Innerchr16:10529441..10641524hg18UCSC Ensembl
Outerchr16:10529441..10641524hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38112084
hg19112084
hg18112084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786417
Samples
Known GenesEMP2, TEKT5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892791
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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