A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878241



Internal ID22653206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45730218..45731717hg38UCSC Ensembl
chr18:43310183..43311682hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478485
Samples
Known GenesSLC14A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878241
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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