A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16963439



Internal ID42948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2198624..2198661hg38UCSC Ensembl
chr5:2198738..2198775hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534671
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16963439
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.007805


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