A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506567



Internal ID283312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56664428..56683901hg38UCSC Ensembl
chr11:56431904..56451377hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3819474
hg1919474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17048240
Samples
Known GenesOR5AR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506567
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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