A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047377



Internal ID18789908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25046172..25081671hg38UCSC Ensembl
Innerchr15:25291319..25326818hg19UCSC Ensembl
Innerchr15:22842412..22877911hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3835500
hg1935500
hg1835500
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2474n100
Supporting Variantsnssv3545398
Samples
Known GenesSNORD116-1, SNORD116-10, SNORD116-11, SNORD116-12, SNORD116-13, SNORD116-14, SNORD116-15, 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)nsv1047377
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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