A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102250



Internal ID21276745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:4413409..4674637hg38UCSC Ensembl
InnerchrY:4281450..4542678hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38261229
hg19261229
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111240
Supporting Variants
Samplessample241
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102250
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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