A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625838



Internal ID21817885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58350195..58350195hg38UCSC Ensembl
chr20:56925251..56925251hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg382734
hg192734
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103717
Supporting Variants
Samples
Known GenesRAB22A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625838
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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