A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059959



Internal ID21969193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152155422..152155422hg38UCSC Ensembl
chr1:152127898..152127898hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17521429
Samples
Known GenesRPTN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059959
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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