A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266812



Internal ID20833852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138301889..138302506hg38UCSC Ensembl
chr5:137637578..137638195hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564658
Supporting Variants
Samples
Known GenesCDC25C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266812
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00038


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