A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958718



Internal ID39789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156660547..156660686hg38UCSC Ensembl
chr4:157581699..157581838hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459114
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958718
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.817983


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