A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169658



Internal ID21313469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25053401..25110682hg38UCSC Ensembl
Outerchr15:25051204..25111187hg38UCSC Ensembl
Innerchr15:25298548..25355829hg19UCSC Ensembl
Outerchr15:25296351..25356334hg19UCSC Ensembl
Innerchr15:22849641..22906922hg18UCSC Ensembl
Outerchr15:22847444..22907427hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3859984
hg1959984
hg1859984
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250768
SamplesNGO_24
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, SNORD116-23, SNORD116-24, SNORD116-25, SNORD116-26, SNORD116-27, SNORD116-28, SNORD116-29, SNORD116-3, SNORD116-4, SNORD116-5, SNORD116-6, SNORD116-7, SNORD116-8, SNORD116-9
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169658
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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