A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622881



Internal ID21814928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53581338..53581338hg38UCSC Ensembl
chr20:52197877..52197877hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104656
Supporting Variants
Samples
Known GenesZNF217
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622881
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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