A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927473



Internal ID22702701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:106309101..106313960hg38UCSC Ensembl
chr9:109071382..109076241hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg384860
hg194860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448854
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927473
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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