A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843757



Internal ID22618692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132618823..132629232hg38UCSC Ensembl
chr6:132939962..132950371hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3810410
hg1910410
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501597
Samples
Known GenesTAAR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843757
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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