A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266607



Internal ID20833647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115698917..115699804hg38UCSC Ensembl
chr5:115034614..115035501hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg38888
hg19888
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566035
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266607
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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