A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923980



Internal ID22699207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128326706..128327010hg38UCSC Ensembl
chr9:131088985..131089289hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439323
Samples
Known GenesCOQ4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923980
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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