A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4010855



Internal ID22072486
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155121
Supporting Variants
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)nssv4010855
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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