A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891474



Internal ID19185870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119977828..120024953hg38UCSC Ensembl
Outerchr8:119977828..120024953hg38UCSC Ensembl
Innerchr8:120990068..121037192hg19UCSC Ensembl
Outerchr8:120990068..121037192hg19UCSC Ensembl
Innerchr8:121059249..121106373hg18UCSC Ensembl
Outerchr8:121059249..121106373hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3847126
hg1947125
hg1847125
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788737
Samples
Known GenesDEPTOR
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891474
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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