A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv960n223



Internal ID22803928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5568264..6075481hg38UCSC Ensembl
chr11:5589494..6096711hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38507218
hg19507218
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6437487, nsv6441849
Samples
Known GenesOR52B6, OR52E4, OR52E6, OR52E8, OR52L1, OR52N1, OR52N2, OR52N4, OR52N5, OR56A1, OR56A3, OR56A4, OR56A5, OR56B1, TRIM22, TRIM34, TRIM5, TRIM6, TRIM6-TRIM34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv960n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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