A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268811



Internal ID20835851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157079670..157080735hg38UCSC Ensembl
chr5:156506681..156507746hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg381066
hg191066
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561207
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268811
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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