A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971464



Internal ID22746399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32785742..32797724hg38UCSC Ensembl
chr18:30365705..30377687hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3811983
hg1911983
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381122
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971464
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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