A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2917785



Internal ID15329389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:147015220..147016628hg38UCSC Ensembl
Innerchr5:146394783..146396191hg19UCSC Ensembl
Innerchr5:146374976..146376384hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381409
hg191409
hg181409
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514327
Supporting Variants
SamplesNA18552
Known GenesPPP2R2B
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2917785
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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