A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892509



Internal ID19183329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40332547..40347758hg38UCSC Ensembl
Outerchr14:40332547..40347758hg38UCSC Ensembl
Innerchr14:40801751..40816962hg19UCSC Ensembl
Outerchr14:40801751..40816962hg19UCSC Ensembl
Innerchr14:39871501..39886712hg18UCSC Ensembl
Outerchr14:39871501..39886712hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3815212
hg1915212
hg1815212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784316
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892509
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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