A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471305



Internal ID21128858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:48131875..49001513hg38UCSC Ensembl
chr11:48153427..49023065hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38869639
hg19869639
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180432
Samples
Known GenesOR4A47, OR4B1, OR4C3, OR4C45, OR4S1, OR4X1, OR4X2, PTPRJ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471305
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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