A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938515



Internal ID26401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108753574..109201574hg38UCSC Ensembl
chr3:108472421..108920421hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38448001
hg19448001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444773
Supporting Variants
Samples
Known GenesFLJ22763, GUCA1C, LINC00488, MORC1, RETNLB, TRAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938515
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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