A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039331



Internal ID18781862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25050690..25090309hg38UCSC Ensembl
Innerchr15:25295837..25335456hg19UCSC Ensembl
Innerchr15:22846930..22886549hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3839620
hg1939620
hg1839620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2476n100
Supporting Variantsnssv3545406
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, SNORD116-3, 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)nsv1039331
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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