A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892368



Internal ID169107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161186559..161186610hg38UCSC Ensembl
chr1:161156349..161156400hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg381155
hg191155
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559759
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892368
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001407


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