A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3551667



Internal ID18752743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:65152360..65153500hg38UCSC Ensembl
Outerchr14:65152342..65153607hg38UCSC Ensembl
Innerchr14:65619078..65620218hg19UCSC Ensembl
Outerchr14:65619060..65620325hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381266
hg191266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9750414
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3551667
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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