A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783737



Internal ID19176331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5902452..5918264hg38UCSC Ensembl
Innerchr10:5944415..5960227hg19UCSC Ensembl
Innerchr10:5984421..6000233hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3815813
hg1915813
hg1815813
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=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783737
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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