A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586488



Internal ID20959559
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 StatusM
Merged Variants
Supporting Variantsnssv18244046
Samples
Known GenesGAREM, MEP1B, RNF125, RNF138, TRAPPC8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586488
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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