A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797339



Internal ID18834397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83038857..83096402hg38UCSC Ensembl
Innerchr16:83072462..83130007hg19UCSC Ensembl
Innerchr16:81629963..81687508hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3857546
hg1957546
hg1857546
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892919
Supporting Variants
Samples
Known GenesCDH13
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=43
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797339
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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