A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535826



Internal ID20909180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:233291342..233292241hg38UCSC Ensembl
chr1:233427088..233427987hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv555n223
Supporting Variantsnssv18250652
Samples
Known GenesPCNXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535826
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