A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268699



Internal ID20835739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150877904..150878968hg38UCSC Ensembl
chr5:150257466..150258530hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg381065
hg191065
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572167
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268699
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