A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244095



Internal ID20811135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13748947..13749882hg38UCSC Ensembl
chr18:13748946..13749881hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38936
hg19936
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579319
Supporting Variants
Samples
Known GenesRNMT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244095
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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