A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051823



Internal ID21961056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239959716..239959716hg38UCSC Ensembl
chr2:240899133..240899133hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528867
Samples
Known GenesNDUFA10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051823
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