A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103202



Internal ID22012435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179633980..179655160hg38UCSC Ensembl
chr5:179060981..179082161hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3821181
hg1921181
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565290
Samples
Known GenesC5orf60
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103202
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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