A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114151



Internal ID21297417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:21366872..21490464hg38UCSC Ensembl
InnerchrY:23528758..23652350hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38123593
hg19123593
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101879
Samplessample64
Known GenesCYorf17, RBMY2EP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114151
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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