A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267582



Internal ID20834622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167596603..167597176hg38UCSC Ensembl
chr5:167023608..167024181hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568782
Supporting Variants
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267582
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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