A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894140



Internal ID19185209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15784929..15795777hg38UCSC Ensembl
Outerchr5:15783391..15801089hg38UCSC Ensembl
Innerchr5:15785038..15795886hg19UCSC Ensembl
Outerchr5:15783500..15801198hg19UCSC Ensembl
Innerchr5:15838038..15848886hg18UCSC Ensembl
Outerchr5:15836500..15854198hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3817699
hg1917699
hg1817699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778750, essv25779748
Samples
Known GenesFBXL7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894140
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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