A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019285



Internal ID21928628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49897697..49898182hg38UCSC Ensembl
chr6:49865410..49865895hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019285
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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