A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060971



Internal ID21970204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30527404..30527404hg38UCSC Ensembl
chr3:30568896..30568896hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542943
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060971
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