A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270239



Internal ID20837279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76993407..76993675hg38UCSC Ensembl
chr5:76289232..76289500hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575207
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270239
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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