A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779748



Internal ID19179609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15784929..15795777hg38UCSC Ensembl
Innerchr5:15785038..15795886hg19UCSC Ensembl
Innerchr5:15838038..15848886hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3810849
hg1910849
hg1810849
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=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779748
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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