A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957669



Internal ID39087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151526287..151526351hg38UCSC Ensembl
chr4:152447439..152447503hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455538
Supporting Variants
Samples
Known GenesFAM160A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957669
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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