A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269193



Internal ID20836233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65667976..65668450hg38UCSC Ensembl
chr5:64963803..64964277hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573029
Supporting Variants
Samples
Known GenesSGTB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269193
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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