A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264073



Internal ID20831113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:917586..1624857hg38UCSC Ensembl
chr3:959269..1666541hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38707272
hg19707273
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541059
Supporting Variants
Samples
Known GenesCNTN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264073
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