A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242588



Internal ID20809628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62568231..62568799hg38UCSC Ensembl
chr17:60645592..60646160hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585136
Supporting Variants
Samples
Known GenesTLK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242588
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00029


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