A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958864



Internal ID39884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158353100..158371935hg38UCSC Ensembl
chr4:159274252..159293087hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3818836
hg1918836
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554040
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958864
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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