A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245192



Internal ID20812232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5107372..5107770hg38UCSC Ensembl
chr17:5010667..5011065hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581599
Supporting Variants
Samples
Known GenesZNF232
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245192
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