A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16967182



Internal ID45434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76310843..76310894hg38UCSC Ensembl
chr5:75606668..75606719hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5408394
Supporting Variants
Samples
Known GenesSV2C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16967182
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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