A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891444



Internal ID19185840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:97374280..97431238hg38UCSC Ensembl
Outerchr8:97374280..97431238hg38UCSC Ensembl
Innerchr8:98386508..98443466hg19UCSC Ensembl
Outerchr8:98386508..98443466hg19UCSC Ensembl
Innerchr8:98455684..98512642hg18UCSC Ensembl
Outerchr8:98455684..98512642hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3856959
hg1956959
hg1856959
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789935
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891444
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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