A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244694



Internal ID20811734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55595261..55595584hg38UCSC Ensembl
chr18:53262492..53262815hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585595
Supporting Variants
Samples
Known GenesTCF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244694
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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