A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3552037



Internal ID18753113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99128277..99128393hg38UCSC Ensembl
Outerchr14:99128265..99128397hg38UCSC Ensembl
Innerchr14:99594614..99594730hg19UCSC Ensembl
Outerchr14:99594602..99594734hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9750784
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3552037
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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