A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055009



Internal ID21964242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:172571982..172571982hg38UCSC Ensembl
chr1:172541122..172541122hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519335
Samples
Known GenesSUCO
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055009
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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