A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015166



Internal ID21924509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125265410..125265677hg38UCSC Ensembl
chr9:128027689..128027956hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591536
Samples
Known GenesGAPVD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015166
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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