A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113237



Internal ID21296503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11016257..11022220hg38UCSC Ensembl
Innerchr10:11058220..11064183hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385964
hg195964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv140n145
Supporting Variantsnssv14089929
Samplessample412
Known GenesCELF2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113237
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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