A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17048213



Internal ID100013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56448372..56470408hg38UCSC Ensembl
chr11:56215848..56237884hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3822037
hg1922037
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555691
Supporting Variants
Samples
Known GenesOR5M3, OR5M9
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17048213
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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