A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16906779



Internal ID5303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98802434..98818909hg38UCSC Ensembl
chr1:99267990..99284465hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3816476
hg1916476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431182
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16906779
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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