A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047190



Internal ID21956424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8865262..8865324hg38UCSC Ensembl
chr21:9754095..9754157hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646878
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047190
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