A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267394



Internal ID20834434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157845078..157845732hg38UCSC Ensembl
chr5:157272086..157272740hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557238
Supporting Variants
Samples
Known GenesCLINT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267394
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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