A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782523



Internal ID18830246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83222772..83381958hg38UCSC Ensembl
Innerchr16:83256377..83415563hg19UCSC Ensembl
Innerchr16:81813878..81973064hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38159187
hg19159187
hg18159187
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892921
Supporting Variants
Samples
Known GenesCDH13
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=102
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782523
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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