A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780895



Internal ID18814645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:112998472..113113216hg38UCSC Ensembl
Innerchr3:112717319..112832063hg19UCSC Ensembl
Innerchr3:114200009..114314753hg18UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38114745
hg19114745
hg18114745
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893763
Supporting Variants
Samples
Known GenesC3orf17, GTPBP8
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780895
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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