A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1003790



Internal ID7068895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:25139479..25147500hg38UCSC Ensembl
Outerchr14:25608685..25616706hg19UCSC Ensembl
Outerchr14:24678525..24686546hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg388022
hg198022
hg188022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565708
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1003790
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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