A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267882



Internal ID20834922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:130477152..130477652hg38UCSC Ensembl
chr5:129812845..129813345hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567913
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267882
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00023


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