A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102266



Internal ID21279756
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 StatusS
Merged Variantsnsv3114436
Supporting Variants
Samplessample289
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102266
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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