A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786519



Internal ID19160481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:361505..380328hg38UCSC Ensembl
Innerchr8:311505..330328hg19UCSC Ensembl
Innerchr8:301505..320328hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3818824
hg1918824
hg1818824
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891249
Supporting Variants
Samples
Known GenesFAM87A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786519
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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