A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929042



Internal ID20071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5114295..5114589hg38UCSC Ensembl
chr3:5155980..5156274hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147496
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929042
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.019201


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