A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589879



Internal ID21781922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4596747..4599047hg38UCSC Ensembl
chr9:4596747..4599047hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg382301
hg192301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001395
Supporting Variants
Samples
Known GenesSPATA6L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589879
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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