A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782737



Internal ID19180840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:121624653..121634407hg38UCSC Ensembl
Innerchr3:121343500..121353254hg19UCSC Ensembl
Innerchr3:122826190..122835944hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg389755
hg199755
hg189755
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893771
Supporting Variants
Samples
Known GenesFBXO40, HCLS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782737
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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