A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891193



Internal ID19185589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:229195933..229202872hg38UCSC Ensembl
Outerchr1:229195933..229205005hg38UCSC Ensembl
Innerchr1:229331680..229338619hg19UCSC Ensembl
Outerchr1:229331680..229340752hg19UCSC Ensembl
Innerchr1:227398303..227405242hg18UCSC Ensembl
Outerchr1:227398303..227407375hg18UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg389073
hg199073
hg189073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796902, essv25796255, essv25797983
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891193
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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