A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295488



Internal ID20504706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:21523013..29424141hg38UCSC Ensembl
chr5:21523122..29424248hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg387901129
hg197901127
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752323
Supporting Variants
Samples
Known GenesCDH10, CDH12, CDH9, GUSBP1, LINC01021, LOC101929681, LOC340107, LSP1P3, PMCHL1, PRDM9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295488
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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