A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962850



Internal ID42555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16464200..16464251hg38UCSC Ensembl
chr5:16464309..16464360hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg386019
hg196019
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560226
Supporting Variants
Samples
Known GenesZNF622
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962850
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005159


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