A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2777747



Internal ID15266522
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 loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514573
Supporting Variants
SamplesNA11893
Known GenesADAMTS14
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2777747
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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