A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962207



Internal ID42102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184507397..184508283hg38UCSC Ensembl
chr4:185428551..185429437hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38887
hg19887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471047
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962207
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004229


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