A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085899



Internal ID21289356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:52351609..52636415hg38UCSC Ensembl
Innerchr8:53264169..53548975hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38284807
hg19284807
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113228
Supporting Variants
Samplessample46
Known GenesFAM150A, RB1CC1, ST18
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085899
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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