A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16906246



Internal ID4960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70410796..70410847hg38UCSC Ensembl
chr1:70876479..70876530hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38812
hg19812
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561506
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16906246
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