A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801497



Internal ID19180272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85557959..85617541hg38UCSC Ensembl
Innerchr8:86470188..86529770hg19UCSC Ensembl
Innerchr8:86657440..86717022hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3859583
hg1959583
hg1859583
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891429
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801497
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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