A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060363



Internal ID21969596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241487588..241487588hg38UCSC Ensembl
chr2:242427003..242427003hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528086
Samples
Known GenesFARP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060363
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