A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2483n100



Internal ID20154099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25170021..25252158hg38UCSC Ensembl
chr15:25415168..25497305hg19UCSC Ensembl
chr15:22966261..23048398hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3882138
hg1982138
hg1882138
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048279, nsv1053067, nsv1050326, nsv1036459, nsv1038602, nsv1040603
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)dgv2483n100
Frequency
Sample Size29084
Observed Gain21
Observed Loss11
Observed Complex0
Frequencyn/a


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