A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892473



Internal ID19183293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22710298..22761937hg38UCSC Ensembl
Outerchr14:22704588..22761937hg38UCSC Ensembl
Innerchr14:23179507..23231146hg19UCSC Ensembl
Outerchr14:23173797..23231146hg19UCSC Ensembl
Innerchr14:22249347..22300986hg18UCSC Ensembl
Outerchr14:22243637..22300986hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3857350
hg1957350
hg1857350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785068, essv25798138, essv25801429, essv25778469, essv25799621, essv25798519
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892473
Frequency
Sample Size3017
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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