A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955962



Internal ID37948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:137556845..137556896hg38UCSC Ensembl
chr4:138477999..138478050hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5406100
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955962
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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