A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891467



Internal ID19185863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:115967306..115976722hg38UCSC Ensembl
Outerchr8:115967306..115976722hg38UCSC Ensembl
Innerchr8:116979531..116988947hg19UCSC Ensembl
Outerchr8:116979531..116988947hg19UCSC Ensembl
Innerchr8:117048709..117058125hg18UCSC Ensembl
Outerchr8:117048709..117058125hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg389417
hg199417
hg189417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786059
Samples
Known GenesLINC00536, MIR6507
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891467
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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