A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893229



Internal ID18837363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48350396..48372932hg38UCSC Ensembl
Outerchr19:48350396..48372932hg38UCSC Ensembl
Innerchr19:48853653..48876189hg19UCSC Ensembl
Outerchr19:48853653..48876189hg19UCSC Ensembl
Innerchr19:53545465..53568001hg18UCSC Ensembl
Outerchr19:53545465..53568001hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3822537
hg1922537
hg1822537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798042
Samples
Known GenesSYNGR4, TMEM143
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893229
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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