A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891442



Internal ID168493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159081782..159081833hg38UCSC Ensembl
chr1:159051572..159051623hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563838
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891442
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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