A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv63n199



Internal ID22802949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179633954..179658566hg38UCSC Ensembl
chr5:179060955..179085567hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3824613
hg1924613
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4751753, nsv4753801
Samples
Known GenesC5orf60
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)dgv63n199
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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