A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033171



Internal ID21942514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55811207..55819004hg38UCSC Ensembl
chr14:56277925..56285722hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg387798
hg197798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033171
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