A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798042



Internal ID18829683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48350396..48372932hg38UCSC Ensembl
Innerchr19:48853653..48876189hg19UCSC Ensembl
Innerchr19:53545465..53568001hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3822537
hg1922537
hg1822537
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893229
Supporting Variants
Samples
Known GenesSYNGR4, TMEM143
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798042
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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