A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111121



Internal ID21294387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:58508619..58514983hg38UCSC Ensembl
Innerchr10:60268379..60274743hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg386365
hg196365
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv164n145
Supporting Variantsnssv14089831
Samplessample365
Known GenesBICC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111121
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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