A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245182



Internal ID20812222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51023833..51024189hg38UCSC Ensembl
chr17:49101194..49101550hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581585
Supporting Variants
Samples
Known GenesSPAG9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245182
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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