A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461321



Internal ID21118874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:48051651..48446171hg38UCSC Ensembl
chr11:48073203..48467723hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38394521
hg19394521
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193275
Samples
Known GenesOR4B1, OR4C3, OR4C45, OR4S1, OR4X1, OR4X2, PTPRJ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461321
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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