A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000213



Internal ID21909556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6013641..6022361hg38UCSC Ensembl
chr5:6013754..6022474hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg388721
hg198721
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000213
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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