A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089856



Internal ID21285330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48303337..48309962hg38UCSC Ensembl
Innerchr10:49511380..49518005hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg386626
hg196626
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118333
Supporting Variants
Samplessample372
Known GenesMAPK8
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089856
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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