A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217469



Internal ID20784509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:47972478..47973027hg38UCSC Ensembl
chr13:48546613..48547162hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38550
hg19550
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576867
Supporting Variants
Samples
Known GenesSUCLA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217469
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00052


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