A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946871



Internal ID31939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11624884..11927293hg38UCSC Ensembl
chr4:11626508..11928917hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38302410
hg19302410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448899
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946871
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