A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969018



Internal ID22743953
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 StatusM
Merged Variants
Supporting Variantsnssv17371835
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969018
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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