A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911005



Internal ID22686217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30045465..30159010hg38UCSC Ensembl
chr9:30045463..30159008hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38113546
hg19113546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448212
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911005
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