A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622234



Internal ID21814281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3788752..3788752hg38UCSC Ensembl
chr20:3769399..3769399hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109553
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622234
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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