A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538016



Internal ID20911342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:109587875..109588504hg38UCSC Ensembl
chr2:110345452..110346081hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4077n223
Supporting Variantsnssv18256473
Samples
Known GenesSEPT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538016
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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