A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756721



Internal ID20532581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:20935423..20940374hg38UCSC Ensembl
chr18:18515384..18520335hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg384952
hg194952
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv49n199
Supporting Variantsnssv16263633
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756721
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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