A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189665



Internal ID20756705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:48198393..48796499hg38UCSC Ensembl
chr11:48219945..48818051hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38598107
hg19598107
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455948
Supporting Variants
Samples
Known GenesOR4A47, OR4B1, OR4C3, OR4C45, OR4S1, OR4X1, OR4X2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189665
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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