A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244853



Internal ID20811893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79057829..79318871hg38UCSC Ensembl
chr18:76817829..77078871hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38261043
hg19261043
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597953
Supporting Variants
Samples
Known GenesATP9B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244853
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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