A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439323



Internal ID22497193
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 StatusS
Merged Variantsnsv5923980
Supporting Variants
Samples
Known GenesCOQ4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439323
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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