A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901759



Internal ID1966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43019686..43031130hg38UCSC Ensembl
chr1:43485357..43496801hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3811445
hg1911445
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555996
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901759
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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