A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891485



Internal ID19185881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:134208362..134407440hg38UCSC Ensembl
Outerchr8:134208362..134407440hg38UCSC Ensembl
Innerchr8:135220605..135419683hg19UCSC Ensembl
Outerchr8:135220605..135419683hg19UCSC Ensembl
Innerchr8:135289787..135488865hg18UCSC Ensembl
Outerchr8:135289787..135488865hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38199079
hg19199079
hg18199079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779377
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891485
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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