A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268376



Internal ID20835416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42788472..42790278hg38UCSC Ensembl
chr5:42788574..42790380hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg381807
hg191807
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571708
Supporting Variants
Samples
Known GenesCCDC152
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268376
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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