A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507522



Internal ID284239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56969523..57004001hg38UCSC Ensembl
chr11:56736998..56771476hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3834479
hg1934479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046964
Samples
Known GenesOR5AK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507522
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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