A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246136



Internal ID20813176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22994039..22994651hg38UCSC Ensembl
chr18:20574002..20574614hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583136
Supporting Variants
Samples
Known GenesRBBP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246136
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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