A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056943



Internal ID21966179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:146045918..146045918hg38UCSC Ensembl
chr2:146803486..146803486hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525268
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056943
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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