A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015059



Internal ID21924402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74467437..74482384hg38UCSC Ensembl
chr6:75177153..75192100hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3814948
hg1914948
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574921
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015059
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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