A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242071



Internal ID20809111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16860746..17015474hg38UCSC Ensembl
chr17:16764060..16918788hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38154729
hg19154729
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576297
Supporting Variants
Samples
Known GenesTNFRSF13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242071
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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