A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787640



Internal ID19166730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:110231786..110290596hg38UCSC Ensembl
Innerchr8:111244015..111302825hg19UCSC Ensembl
Innerchr8:111313191..111372001hg18UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3858811
hg1958811
hg1858811
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891457
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787640
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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