A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780711



Internal ID18828792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25172277..25204291hg38UCSC Ensembl
Innerchr8:25029792..25061807hg19UCSC Ensembl
Innerchr8:25085709..25117724hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3832015
hg1932016
hg1832016
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891378
Supporting Variants
Samples
Known GenesDOCK5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780711
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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