A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006123



Internal ID21915466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111272225..111272312hg38UCSC Ensembl
chr6:111593428..111593515hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572374
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006123
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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