A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784695



Internal ID18814764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:5832198..5839735hg38UCSC Ensembl
Innerchr19:5832209..5839746hg19UCSC Ensembl
Innerchr19:5783209..5790746hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg387538
hg197538
hg187538
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893160
Supporting Variants
Samples
Known GenesFUT6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784695
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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