A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2777858



Internal ID15443759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70689222..70690174hg38UCSC Ensembl
Innerchr10:72448978..72449930hg19UCSC Ensembl
Innerchr10:72118984..72119936hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38953
hg19953
hg18953
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514573
Supporting Variants
SamplesNA21438
Known GenesADAMTS14
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2777858
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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