A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892323



Internal ID19183143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:31954821..31961151hg38UCSC Ensembl
Outerchr13:31954821..31961859hg38UCSC Ensembl
Innerchr13:32528958..32535288hg19UCSC Ensembl
Outerchr13:32528958..32535996hg19UCSC Ensembl
Innerchr13:31426958..31433288hg18UCSC Ensembl
Outerchr13:31426958..31433996hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg387039
hg197039
hg187039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784159, essv25781104, essv25786434, essv25783637, essv25780340, essv25783689, essv25781317, essv25782089, essv25780629, essv25783931, essv25779949, essv25798232, essv25781057, essv25784342, essv25781660, essv25780583, essv25784370, essv25785754
Samples
Known GenesEEF1DP3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892323
Frequency
Sample Size3017
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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