A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266485



Internal ID20833525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:104224313..105606635hg38UCSC Ensembl
chr5:103560014..104942336hg19UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg381382323
hg191382323
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574306
Supporting Variants
Samples
Known GenesRAB9BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266485
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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