A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244894



Internal ID20811934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21574057..22827414hg38UCSC Ensembl
chr19:21756859..23010216hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381253358
hg191253358
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599687
Supporting Variants
Samples
Known GenesLOC100996349, LOC440518, LOC641367, ZNF100, ZNF208, ZNF257, ZNF43, ZNF492, ZNF676, ZNF729, ZNF98, ZNF99
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244894
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.02391


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