A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110290



Internal ID21293556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:18674215..18873549hg38UCSC Ensembl
InnerchrY:20836101..21035435hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg38199335
hg19199335
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1294n145
Supporting Variantsnssv14101878
Samplessample53
Known GenesHSFY1, HSFY2, NCRNA00185, TTTY9A, TTTY9B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110290
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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