A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057999



Internal ID21967232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:12965809..12981027hg38UCSC Ensembl
chr21:14338130..14353348hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3815219
hg1915219
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641317
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057999
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