A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112886



Internal ID21296152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:125213637..125265754hg38UCSC Ensembl
Innerchr6:125534783..125586900hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3852118
hg1952118
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083963, nssv14087857
Samplessample256, sample418
Known GenesTPD52L1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112886
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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