A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468197



Internal ID22526086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124015473..124025121hg38UCSC Ensembl
chr11:123886180..123895828hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg389649
hg199649
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864597
Supporting Variants
Samples
Known GenesOR10G4, OR10G9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468197
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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