A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013828



Internal ID21923171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159710680..159712772hg38UCSC Ensembl
chr6:160131712..160133804hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382093
hg192093
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013828
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