A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028563



Internal ID86739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121583094..121589404hg38UCSC Ensembl
chr9:124345373..124351683hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg386311
hg196311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487726
Supporting Variants
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028563
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