A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113752



Internal ID21297018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:22215341..22726851hg38UCSC Ensembl
InnerchrY:24361488..24872998hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38511511
hg19511511
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102295
Samplessample381
Known GenesLOC100652931, PRY, PRY2, RBMY1F, RBMY1J, RBMY2FP, TTTY5, TTTY6, TTTY6B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113752
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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