A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014751



Internal ID21924094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27839447..27843914hg38UCSC Ensembl
chr6:27807225..27811692hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg384468
hg194468
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576642
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014751
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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