A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3552076



Internal ID18406466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102178152..102179642hg38UCSC Ensembl
Outerchr14:102178122..102179898hg38UCSC Ensembl
Innerchr14:102644489..102645979hg19UCSC Ensembl
Outerchr14:102644459..102646235hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381777
hg191777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9750823
Samples
Known GenesWDR20
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3552076
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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