A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16889902



Internal ID167376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:115923639..115923705hg38UCSC Ensembl
chr1:116466260..116466326hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139075
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16889902
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.213759


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