A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3551792



Internal ID18752868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76531746..76532763hg38UCSC Ensembl
Outerchr14:76531573..76532822hg38UCSC Ensembl
Innerchr14:76998089..76999106hg19UCSC Ensembl
Outerchr14:76997916..76999165hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381250
hg191250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9750539
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3551792
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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