A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891406



Internal ID18839116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:61776965..62523810hg38UCSC Ensembl
Outerchr8:61776965..62523810hg38UCSC Ensembl
Innerchr8:62689524..63436369hg19UCSC Ensembl
Outerchr8:62689524..63436369hg19UCSC Ensembl
Innerchr8:62852078..63598923hg18UCSC Ensembl
Outerchr8:62852078..63598923hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38746846
hg19746846
hg18746846
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792930
Samples
Known GenesNKAIN3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891406
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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