A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055745



Internal ID21964978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63086018..63086018hg38UCSC Ensembl
chr2:63313153..63313153hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38716
hg19716
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532899
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055745
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