A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266696



Internal ID20833736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134007166..134301352hg38UCSC Ensembl
chr5:133342857..133637043hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38294187
hg19294187
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569546
Supporting Variants
Samples
Known GenesCDKL3, MIR3661, PPP2CA, SKP1, TCF7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266696
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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