A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468412



Internal ID22526301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124020985..124029969hg38UCSC Ensembl
chr11:123891692..123900676hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg388985
hg198985
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867243
Supporting Variants
Samples
Known GenesOR10G8, OR10G9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468412
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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