A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114436



Internal ID21297702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:21028200..21047615hg38UCSC Ensembl
InnerchrY:23190086..23209501hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3819416
hg1919416
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102266
Samplessample289
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114436
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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