A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244177



Internal ID20811217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3427885..3428458hg38UCSC Ensembl
chr18:3427883..3428456hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595231
Supporting Variants
Samples
Known GenesTGIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244177
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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