A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892506



Internal ID19183326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40017140..40072276hg38UCSC Ensembl
Outerchr14:39974395..40072276hg38UCSC Ensembl
Innerchr14:40486344..40541480hg19UCSC Ensembl
Outerchr14:40443599..40541480hg19UCSC Ensembl
Innerchr14:39556095..39611231hg18UCSC Ensembl
Outerchr14:39513350..39611231hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3897882
hg1997882
hg1897882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782508, essv25800161
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892506
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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