A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058779



Internal ID21968012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:163260342..163260342hg38UCSC Ensembl
chr1:163230132..163230132hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519238
Samples
Known GenesRGS5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058779
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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