A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976313



Internal ID51604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147865817..147872188hg38UCSC Ensembl
chr5:147245380..147251751hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg386372
hg196372
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554771
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976313
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.241805


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