A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217228



Internal ID20784268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99007387..99008273hg38UCSC Ensembl
chr13:99659641..99660527hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38887
hg19887
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577380
Supporting Variants
Samples
Known GenesDOCK9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217228
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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