A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260336



Internal ID20827376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136557564..136558404hg38UCSC Ensembl
chr3:136276406..136277246hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38841
hg19841
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558549
Supporting Variants
Samples
Known GenesSTAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260336
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