A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233977



Internal ID20801018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34756474..34757403hg38UCSC Ensembl
chr14:35225680..35226609hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38930
hg19930
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583688
Supporting Variants
Samples
Known GenesBAZ1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233977
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer