A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059236



Internal ID21968470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:217805612..217805612hg38UCSC Ensembl
chr2:218670335..218670335hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524021
Samples
Known GenesTNS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059236
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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