A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060688



Internal ID21969921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28430055..28430055hg38UCSC Ensembl
chr6:28397832..28397832hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575139
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060688
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer