A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891839



Internal ID168755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168636558..168637423hg38UCSC Ensembl
chr1:168605796..168606661hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38866
hg19866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418216
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891839
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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