A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271848



Internal ID20481066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11509272..11511386hg38UCSC Ensembl
chr18:11509271..11511385hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg382115
hg192115
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758703
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271848
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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