A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691344



Internal ID115010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:70621361..70638522hg38UCSC Ensembl
chr13:71195493..71212654hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3817162
hg1917162
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554346
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691344
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