A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893380



Internal ID19184200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:17337244..17419399hg38UCSC Ensembl
Outerchr21:17334685..17436605hg38UCSC Ensembl
Innerchr21:18709563..18791718hg19UCSC Ensembl
Outerchr21:18707004..18808923hg19UCSC Ensembl
Innerchr21:17631434..17713589hg18UCSC Ensembl
Outerchr21:17628875..17730794hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38101921
hg19101920
hg18101920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797018, essv25796400
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893380
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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