A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560023



Internal ID22428818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25609534..25609534hg38UCSC Ensembl
chr13:26183672..26183672hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14367420, nssv14367421, nssv14367419
SamplesHG00731, HG00732, HG00733
Known GenesATP8A2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560023
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer