A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012464



Internal ID21921807
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 StatusM
Merged Variants
Supporting Variantsnssv17586148
Samples
Known GenesSLC24A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012464
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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