A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057952



Internal ID21967185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:217809171..217809171hg38UCSC Ensembl
chr2:218673894..218673894hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528173
Samples
Known GenesTNS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057952
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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