A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054201



Internal ID21963434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14311764..14311764hg38UCSC Ensembl
chr3:14353264..14353264hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548088
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054201
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