A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048551



Internal ID21957784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58350440..58350717hg38UCSC Ensembl
chr20:56925496..56925773hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629209
Samples
Known GenesRAB22A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048551
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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