A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591590



Internal ID20964661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32056403..32057334hg38UCSC Ensembl
chr18:29636366..29637297hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38932
hg19932
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244064
Samples
Known GenesRNF125
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591590
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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