A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945090



Internal ID30723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8609134..8609148hg38UCSC Ensembl
chr4:8610861..8610875hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542863
Supporting Variants
Samples
Known GenesCPZ
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945090
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.044004


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