A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054358



Internal ID21963591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118263058..118263058hg38UCSC Ensembl
chr1:118805681..118805681hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522671
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054358
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