A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799236



Internal ID18832019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82679946..82693813hg38UCSC Ensembl
Innerchr16:82713551..82727418hg19UCSC Ensembl
Innerchr16:81271052..81284919hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3813868
hg1913868
hg1813868
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892917
Supporting Variants
Samples
Known GenesCDH13, MIR8058
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799236
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer