A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262567



Internal ID20829607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148759811..148762084hg38UCSC Ensembl
chr3:148477598..148479871hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg382274
hg192274
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572819
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262567
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