A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746282



Internal ID20522294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113453112..113453249hg38UCSC Ensembl
chr9:116215392..116215529hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273339
Samples
Known GenesRGS3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746282
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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