A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067980



Internal ID21977213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2341257..2341257hg38UCSC Ensembl
chr5:2341371..2341371hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553565
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067980
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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