A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2777424



Internal ID15610804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130465498..130521138hg38UCSC Ensembl
Innerchr10:132263762..132319402hg19UCSC Ensembl
Innerchr10:132153752..132209392hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3855641
hg1955641
hg1855641
Variant TypeCNV gain
Copy Number16
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514544
Supporting Variants
SamplesNA11840
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2777424
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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