A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117075



Internal ID21300341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:4685711..5103723hg38UCSC Ensembl
InnerchrY:4553752..4971764hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38418013
hg19418013
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102249
Samplessample235
Known GenesPCDH11Y
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117075
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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