A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16907717



Internal ID5925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:112157835..112203835hg38UCSC Ensembl
chr1:112700457..112746457hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3846001
hg1946001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414451
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16907717
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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