A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057793



Internal ID21967026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32723063..32724967hg38UCSC Ensembl
chr20:31310870..31312774hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381905
hg191905
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625910
Samples
Known GenesCOMMD7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057793
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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