A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765760



Internal ID20541620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:20933769..20940254hg38UCSC Ensembl
chr18:18513730..18520215hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg386486
hg196486
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv49n199
Supporting Variantsnssv16280328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765760
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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