A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797856



Internal ID18824782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:42329007..43025374hg38UCSC Ensembl
Innerchr20:40957647..41654014hg19UCSC Ensembl
Innerchr20:40391061..41087428hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38696368
hg19696368
hg18696368
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893336
Supporting Variants
Samples
Known GenesPTPRT
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=221
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797856
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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