A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024663



Internal ID84177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36458500..36467000hg38UCSC Ensembl
chr9:36458497..36466997hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg388501
hg198501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492688
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024663
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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