A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781698



Internal ID19171890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5902452..5919135hg38UCSC Ensembl
Innerchr10:5944415..5961098hg19UCSC Ensembl
Innerchr10:5984421..6001104hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3816684
hg1916684
hg1816684
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891745
Supporting Variants
Samples
Known GenesFBXO18
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781698
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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