A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244046



Internal ID20811086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31938930..32318379hg38UCSC Ensembl
chr18:29518893..29898342hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38379450
hg19379450
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586488
Supporting Variants
Samples
Known GenesGAREM, MEP1B, RNF125, RNF138, TRAPPC8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244046
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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