A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946975



Internal ID32007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22238987..22239019hg38UCSC Ensembl
chr4:22240610..22240642hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381552
hg191552
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555860
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946975
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001874


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