A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2474n100



Internal ID19012842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25046172..25083568hg38UCSC Ensembl
chr15:25291319..25328715hg19UCSC Ensembl
chr15:22842412..22879808hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3837397
hg1937397
hg1837397
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048183, nsv1048439, nsv1047377, nsv1036932
Samples
Known GenesSNORD116-1, SNORD116-10, SNORD116-11, SNORD116-12, SNORD116-13, SNORD116-14, SNORD116-15, SNORD116-16, SNORD116-2, 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)dgv2474n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer