A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892573



Internal ID19183393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:87019995..87029029hg38UCSC Ensembl
Outerchr14:87019995..87029029hg38UCSC Ensembl
Innerchr14:87486339..87495373hg19UCSC Ensembl
Outerchr14:87486339..87495373hg19UCSC Ensembl
Innerchr14:86556092..86565126hg18UCSC Ensembl
Outerchr14:86556092..86565126hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg389035
hg199035
hg189035
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786398
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892573
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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