A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261301



Internal ID20828341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28334052..28335073hg38UCSC Ensembl
chr3:28375543..28376564hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg381022
hg191022
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546148
Supporting Variants
Samples
Known GenesAZI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261301
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