A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894139



Internal ID19185208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15702360..15719241hg38UCSC Ensembl
Outerchr5:15702360..15719241hg38UCSC Ensembl
Innerchr5:15702469..15719350hg19UCSC Ensembl
Outerchr5:15702469..15719350hg19UCSC Ensembl
Innerchr5:15755469..15772350hg18UCSC Ensembl
Outerchr5:15755469..15772350hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3816882
hg1916882
hg1816882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781373
Samples
Known GenesFBXL7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894139
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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