A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474975



Internal ID252624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99721451..99723712hg38UCSC Ensembl
chr9:102483733..102485994hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg382262
hg192262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025524
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474975
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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