A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371721



Internal ID22597390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38841745..38846542hg38UCSC Ensembl
chr18:36421709..36426506hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg384798
hg194798
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978861
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371721
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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