A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756723



Internal ID20532583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:20930940..20939791hg38UCSC Ensembl
chr18:18510901..18519752hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg388852
hg198852
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296599
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756723
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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