A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261374



Internal ID20828414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32144853..32145187hg38UCSC Ensembl
chr3:32186345..32186679hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539882
Supporting Variants
Samples
Known GenesGPD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261374
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