A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891026



Internal ID168193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158219293..158233943hg38UCSC Ensembl
chr1:158189083..158203733hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3814651
hg1914651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423354
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891026
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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