A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892921



Internal ID18837055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83222772..83381958hg38UCSC Ensembl
Outerchr16:83222772..83381958hg38UCSC Ensembl
Innerchr16:83256377..83415563hg19UCSC Ensembl
Outerchr16:83256377..83415563hg19UCSC Ensembl
Innerchr16:81813878..81973064hg18UCSC Ensembl
Outerchr16:81813878..81973064hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38159187
hg19159187
hg18159187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782523
Samples
Known GenesCDH13
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892921
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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