A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617148



Internal ID20990219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131559809..131560134hg38UCSC Ensembl
chr6:131880949..131881274hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215563
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617148
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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