A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244478



Internal ID20811518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48806751..48807252hg38UCSC Ensembl
chr17:46884113..46884614hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585598
Supporting Variants
Samples
Known GenesTTLL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244478
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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