A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008567



Internal ID21917910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:84203133..84484305hg38UCSC Ensembl
chr9:86818048..87099220hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38281173
hg19281173
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592181
Samples
Known GenesSLC28A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008567
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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