A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567615



Internal ID16008338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20852957..20946340hg38UCSC Ensembl
Innerchr15:21058286..21151669hg19UCSC Ensembl
Innerchr15:19322874..19416328hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3893384
hg1993384
hg1893455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4238n54
Supporting Variantsnssv837491
Samples
Known GenesCT60, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567615
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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