A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059716



Internal ID21968949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43301879..43308320hg38UCSC Ensembl
chr20:41930519..41936960hg19UCSC Ensembl
Cytoband20q13.11
Allele length
AssemblyAllele length
hg386442
hg196442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626030
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059716
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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