A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404129



Internal ID22461999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:55959027..55959027hg38UCSC Ensembl
chr20:54534083..54534083hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977119
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404129
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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