A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111853



Internal ID22021087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8237512..8237512hg38UCSC Ensembl
chrUn_gl000220:135937..135937hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643707
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111853
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