A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072859



Internal ID21982092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122726893..122726893hg38UCSC Ensembl
chr3:122445740..122445740hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548168
Samples
Known GenesPARP14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072859
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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