A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957387



Internal ID38908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:136593620..136608272hg38UCSC Ensembl
chr4:137514775..137529427hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3814653
hg1914653
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460335
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957387
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