A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733463



Internal ID157129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61153375..61153375hg38UCSC Ensembl
chr20:59728431..59728431hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381660
hg191660
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5549775
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733463
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.053275


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