A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2479n100



Internal ID20154095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25165723..25261420hg38UCSC Ensembl
chr15:25410870..25506567hg19UCSC Ensembl
chr15:22961963..23057660hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3895698
hg1995698
hg1895698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046240, nsv1035247, nsv1052476, nsv1040827, nsv1053273, nsv1054596, nsv1048047, nsv1036088, nsv1039770, nsv1039667, nsv1046244, nsv1040947, nsv1039263, nsv1048719, nsv1052429, nsv1038230, nsv1047275, nsv1047959, nsv1043447, nsv1040437, nsv1041695, nsv1051342, nsv1053230, nsv1047240, nsv1037848, nsv1045286, nsv1046574, nsv1052121, nsv1039253, nsv1053345, nsv1037643, nsv1048479, nsv1050869, nsv1041030, nsv1039489, nsv1043993, nsv1054884, nsv1042447
Samples
Known GenesPWAR4, SNORD115-1, SNORD115-10, SNORD115-11, SNORD115-12, SNORD115-13, SNORD115-14, SNORD115-15, SNORD115-16, SNORD115-17, SNORD115-18, SNORD115-19, SNORD115-2, SNORD115-20, SNORD115-21, SNORD115-22, SNORD115-23, SNORD115-24, SNORD115-25, SNORD115-26, SNORD115-27, SNORD115-28, SNORD115-29, SNORD115-3, SNORD115-30, SNORD115-31, SNORD115-32, SNORD115-33, SNORD115-34, SNORD115-35, SNORD115-36, SNORD115-37, SNORD115-38, SNORD115-39, SNORD115-4, SNORD115-40, SNORD115-41, SNORD115-42, SNORD115-43, SNORD115-44, SNORD115-5, SNORD115-6, SNORD115-7, SNORD115-8, SNORD115-9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2479n100
Frequency
Sample Size29084
Observed Gain98
Observed Loss0
Observed Complex0
Frequencyn/a


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