A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013201



Internal ID21922544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27270514..27270577hg38UCSC Ensembl
chr6:27238293..27238356hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561657
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013201
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