A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892384



Internal ID19183204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:69070840..69110716hg38UCSC Ensembl
Outerchr13:69066747..69121961hg38UCSC Ensembl
Innerchr13:69644972..69684848hg19UCSC Ensembl
Outerchr13:69640879..69696093hg19UCSC Ensembl
Innerchr13:68542973..68582849hg18UCSC Ensembl
Outerchr13:68538880..68594094hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3855215
hg1955215
hg1855215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784706, essv25779723, essv25782987, essv25797818, essv25800098
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892384
Frequency
Sample Size3017
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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