A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844283



Internal ID22619218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132608341..132611777hg38UCSC Ensembl
chr6:132929480..132932916hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg383437
hg193437
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501724
Samples
Known GenesTAAR3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844283
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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