A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792960



Internal ID19163849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131437926..131888690hg38UCSC Ensembl
Innerchr8:132450173..132900937hg19UCSC Ensembl
Innerchr8:132519355..132970119hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38450765
hg19450765
hg18450765
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891484
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=87
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792960
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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