A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922438



Internal ID22697663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21452740..21489024hg38UCSC Ensembl
chr9:21452739..21489023hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3836285
hg1936285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443122
Samples
Known GenesIFNE, MIR31HG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922438
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