A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266801



Internal ID20833841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138108439..138108992hg38UCSC Ensembl
chr5:137444128..137444681hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567632
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266801
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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