A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051105



Internal ID21960339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218352775..218352775hg38UCSC Ensembl
chr2:219217498..219217498hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg382619
hg192619
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518334
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051105
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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