A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006467



Internal ID21915810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49432367..49570406hg38UCSC Ensembl
chr6:49400080..49538119hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38138040
hg19138040
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577019
Samples
Known GenesC6orf141, CENPQ, GLYATL3, MUT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006467
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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