A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504418



Internal ID22562361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27909862..27911293hg38UCSC Ensembl
chr6:27877640..27879071hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381432
hg191432
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844588
Supporting Variants
Samples
Known GenesOR2B2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504418
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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