A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088708



Internal ID21278751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11015525..11020735hg38UCSC Ensembl
Innerchr10:11057488..11062698hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385211
hg195211
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111085
Supporting Variants
Samplessample273
Known GenesCELF2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088708
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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