A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058150



Internal ID21967384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:163238504..163238504hg38UCSC Ensembl
chr1:163208294..163208294hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg382248
hg192248
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532343
Samples
Known GenesRGS5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058150
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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