A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269198



Internal ID20836238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65719307..65720334hg38UCSC Ensembl
chr5:65015134..65016161hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg381028
hg191028
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569104
Supporting Variants
Samples
Known GenesSGTB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269198
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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