A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16950884



Internal ID34623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46885068..46890138hg38UCSC Ensembl
chr4:46887085..46892155hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg385071
hg195071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463970
Supporting Variants
Samples
Known GenesCOX7B2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16950884
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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