A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961909



Internal ID41907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6350680..6355845hg38UCSC Ensembl
chr5:6350793..6355958hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385166
hg195166
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557047
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961909
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.002185


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