A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080051



Internal ID21989284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40556608..40556608hg38UCSC Ensembl
chr5:40556710..40556710hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544888
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080051
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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