A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16960867



Internal ID41222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2058586..2070037hg38UCSC Ensembl
chr5:2058700..2070151hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3811452
hg1911452
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147235
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16960867
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.08133


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