A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2476n100



Internal ID20154092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25050690..25092283hg38UCSC Ensembl
chr15:25295837..25337430hg19UCSC Ensembl
chr15:22846930..22888523hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3841594
hg1941594
hg1841594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044599, nsv1039331
Samples
Known GenesSNORD116-1, SNORD116-10, SNORD116-11, SNORD116-12, SNORD116-13, SNORD116-14, SNORD116-15, SNORD116-16, SNORD116-17, SNORD116-18, SNORD116-19, SNORD116-2, SNORD116-20, SNORD116-21, SNORD116-22, SNORD116-23, SNORD116-3, SNORD116-4, SNORD116-5, SNORD116-6, SNORD116-7, SNORD116-8, SNORD116-9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2476n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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