A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2815495



Internal ID15738150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24861870..24863546hg38UCSC Ensembl
Innerchr15:25107017..25108693hg19UCSC Ensembl
Innerchr15:22658110..22659786hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381677
hg191677
hg181677
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514772
Supporting Variants
SamplesNA19128
Known GenesSNRPN
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2815495
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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