A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16948645



Internal ID33132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28589287..28626274hg38UCSC Ensembl
chr4:28590909..28627896hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3836988
hg1936988
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556099
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16948645
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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