A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753801



Internal ID20529661
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 Variantsdgv63n199
Supporting Variantsnssv16287862
Samples
Known GenesC5orf60
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753801
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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