A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024969



Internal ID84377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90994552..91000552hg38UCSC Ensembl
chr9:93756834..93762834hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484509
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024969
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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