A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543127



Internal ID20916378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:193098263..193098826hg38UCSC Ensembl
chr1:193067393..193067956hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250244
Samples
Known GenesGLRX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543127
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