A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977632



Internal ID52478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172627819..172627819hg38UCSC Ensembl
chr5:172054822..172054822hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38472
hg19472
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539465
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977632
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.045469


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