A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778750



Internal ID19173905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15783391..15801089hg38UCSC Ensembl
Innerchr5:15783500..15801198hg19UCSC Ensembl
Innerchr5:15836500..15854198hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3817699
hg1917699
hg1817699
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894140
Supporting Variants
Samples
Known GenesFBXL7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778750
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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