A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117247



Internal ID21300513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:3609519..4774496hg38UCSC Ensembl
InnerchrY:3477560..4642537hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg381164978
hg191164978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102236
Samplessample206
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117247
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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