A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920228



Internal ID22695451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129043791..129044083hg38UCSC Ensembl
chr9:131806070..131806362hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446662
Samples
Known GenesFAM73B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920228
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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