A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046487



Internal ID98798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72121325..72121339hg38UCSC Ensembl
chr11:71832371..71832385hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535515
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046487
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.088636


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