A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114849



Internal ID21298115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11806955..11858328hg38UCSC Ensembl
Innerchr10:11848954..11900327hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3851374
hg1951374
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv142n145
Supporting Variantsnssv14088735
Samplessample292
Known GenesPROSER2, PROSER2-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114849
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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