A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229917



Internal ID20796958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106562898..106563000hg38UCSC Ensembl
chr13:107215246..107215348hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585783
Supporting Variants
Samples
Known GenesARGLU1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229917
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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