A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16967515



Internal ID45657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72491129..72491129hg38UCSC Ensembl
chr5:71786956..71786956hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg381
hg191
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555006
Supporting Variants
Samples
Known GenesZNF366
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16967515
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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