A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016078



Internal ID21925421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49565084..49567835hg38UCSC Ensembl
chr6:49532797..49535548hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg382752
hg192752
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567097
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016078
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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