A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891491



Internal ID19185887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139008777..139029794hg38UCSC Ensembl
Outerchr8:139008777..139029794hg38UCSC Ensembl
Innerchr8:140021020..140042037hg19UCSC Ensembl
Outerchr8:140021020..140042037hg19UCSC Ensembl
Innerchr8:140090202..140111219hg18UCSC Ensembl
Outerchr8:140090202..140111219hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3821018
hg1921018
hg1821018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781049
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891491
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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