A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567328



Internal ID20940399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154434144..154438031hg38UCSC Ensembl
chr5:153813704..153817591hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg383888
hg193888
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268747
Samples
Known GenesSAP30L-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567328
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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