A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371835



Internal ID22597504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:28881561..28883942hg38UCSC Ensembl
chr18:26461526..26463907hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg382382
hg192382
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969018
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371835
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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