A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242495



Internal ID20809535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:47738647..47739521hg38UCSC Ensembl
chr17:45816013..45816887hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589730
Supporting Variants
Samples
Known GenesTBX21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242495
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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