A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051409



Internal ID19140628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25174833..25215819hg38UCSC Ensembl
Innerchr15:25419980..25460966hg19UCSC Ensembl
Innerchr15:22971073..23012059hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3840987
hg1940987
hg1840987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2481n100
Supporting Variantsnssv3545581
Samples
Known GenesPWAR4, SNORD115-10, SNORD115-11, SNORD115-12, SNORD115-13, SNORD115-14, SNORD115-15, SNORD115-16, SNORD115-17, SNORD115-18, SNORD115-19, SNORD115-20, SNORD115-21, SNORD115-22, SNORD115-23, SNORD115-24, SNORD115-25, SNORD115-29, SNORD115-3, SNORD115-36, SNORD115-4, SNORD115-43, 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)nsv1051409
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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