A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250245



Internal ID20817285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:193099336..193100496hg38UCSC Ensembl
chr1:193068466..193069626hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg381161
hg191161
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537202
Supporting Variants
Samples
Known GenesGLRX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250245
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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