A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845086



Internal ID22620021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20172993..20177492hg38UCSC Ensembl
chr6:20173224..20177723hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503763
Samples
Known GenesMBOAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845086
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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