A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567632



Internal ID16008355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20873524..20956011hg38UCSC Ensembl
Innerchr15:21078853..21161340hg19UCSC Ensembl
Innerchr15:19343513..19425999hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3882488
hg1982488
hg1882487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4238n54
Supporting Variantsnssv837509
Samples
Known GenesCT60, NF1P2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567632
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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