A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026830



Internal ID85607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96733078..96742906hg38UCSC Ensembl
chr9:99495360..99505188hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg389829
hg199829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474226
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026830
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