A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155121



Internal ID22085626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25145857..25185096hg38UCSC Ensembl
Outerchr15:25143120..25188158hg38UCSC Ensembl
Innerchr15:25391004..25430243hg19UCSC Ensembl
Outerchr15:25388267..25433305hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3845039
hg1945039
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010855
Samples
Known GenesSNORD115-1, SNORD115-10, SNORD115-12, SNORD115-2, SNORD115-3, SNORD115-4, SNORD115-5, SNORD115-6, SNORD115-7, SNORD115-8, SNORD115-9
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155121
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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