A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023047



Internal ID83074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61965500..62082634hg38UCSC Ensembl
chr9:45101652..45218786hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38117135
hg19117135
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142674
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023047
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008475


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