A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111566



Internal ID21294832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:22208726..22376449hg38UCSC Ensembl
InnerchrY:24354873..24522596hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38167724
hg19167724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102292, nssv14102298
Samplessample369, sample387
Known GenesLOC100652931, RBMY1F, RBMY2FP, TTTY5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111566
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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