A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089831



Internal ID21284831
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 StatusS
Merged Variantsnsv3111121
Supporting Variants
Samplessample365
Known GenesBICC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089831
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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