A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536045



Internal ID20909398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154007444..154008408hg38UCSC Ensembl
chr1:153979920..153980884hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38965
hg19965
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247067
Samples
Known GenesNUP210L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536045
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