A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441849



Internal ID21099402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5588812..6011442hg38UCSC Ensembl
chr11:5610042..6032672hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38422631
hg19422631
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv960n223
Supporting Variantsnssv18194036
Samples
Known GenesOR52E4, OR52E6, OR52E8, OR52L1, OR52N1, OR52N2, OR52N4, OR52N5, OR56A3, OR56A4, OR56A5, OR56B1, TRIM22, TRIM34, TRIM5, TRIM6, TRIM6-TRIM34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441849
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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