A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247699



Internal ID20814739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36578673..36579066hg38UCSC Ensembl
chr19:37069575..37069968hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597410
Supporting Variants
Samples
Known GenesZNF529
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247699
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