A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4238n54



Internal ID18996414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20852957..20956011hg38UCSC Ensembl
chr15:21058286..21161340hg19UCSC Ensembl
chr15:19322874..19425999hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38103055
hg19103055
hg18103126
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv567615, nsv567632
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)dgv4238n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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