A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586148



Internal ID21778191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19648291..19701921hg38UCSC Ensembl
chr9:19648289..19701919hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3853631
hg1953631
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012464
Supporting Variants
Samples
Known GenesSLC24A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586148
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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