A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901403



Internal ID1750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33224903..33244204hg38UCSC Ensembl
chr1:33690504..33709805hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3819302
hg1919302
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561045
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901403
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