A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2812547



Internal ID15750428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24824386..24837354hg38UCSC Ensembl
Innerchr15:25069533..25082501hg19UCSC Ensembl
Innerchr15:22620626..22633594hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3812969
hg1912969
hg1812969
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514771
Supporting Variants
SamplesNA19173
Known GenesSNRPN
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2812547
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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