A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844282



Internal ID22619217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132353310..132359656hg38UCSC Ensembl
chr6:132674449..132680795hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg386347
hg196347
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501596
Samples
Known GenesMOXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844282
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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