A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042782



Internal ID21952094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98435567..98435567hg38UCSC Ensembl
chr2:99052030..99052030hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524081
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042782
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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