A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903669



Internal ID3263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32934456..32934506hg38UCSC Ensembl
chr1:33400057..33400107hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541057
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903669
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer