A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110858



Internal ID21294124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:3249400..3295612hg38UCSC Ensembl
InnerchrY:3117441..3163653hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3846213
hg1946213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102247
Samplessample235
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110858
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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