A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020863



Internal ID21930206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87089542..87089864hg38UCSC Ensembl
chr14:87555886..87556208hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020863
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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