A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911032



Internal ID22686244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4710326..4909311hg38UCSC Ensembl
chr9:4710326..4909311hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38198986
hg19198986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441155
Samples
Known GenesAK3, MIR101-2, RCL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911032
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