A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269694



Internal ID20836734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87221092..87221546hg38UCSC Ensembl
chr5:86516909..86517363hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568909
Supporting Variants
Samples
Known GenesLOC101929380
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269694
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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