A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060808



Internal ID21970041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133785405..133785405hg38UCSC Ensembl
chr3:133504249..133504249hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541610
Samples
Known GenesSRPRB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060808
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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