A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796361



Internal ID18828454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82931460..83009567hg38UCSC Ensembl
Innerchr16:82965065..83043172hg19UCSC Ensembl
Innerchr16:81522566..81600673hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3878108
hg1978108
hg1878108
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892918
Supporting Variants
Samples
Known GenesCDH13
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=26
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796361
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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