A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568550



Internal ID16355959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25153197..25204590hg38UCSC Ensembl
Innerchr15:25398344..25449737hg19UCSC Ensembl
Innerchr15:22949437..23000830hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3851394
hg1951394
hg1851394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149219
SamplesNINDS_184
Known GenesSNORD115-1, SNORD115-10, SNORD115-11, SNORD115-12, SNORD115-13, SNORD115-14, SNORD115-15, SNORD115-16, SNORD115-17, SNORD115-18, SNORD115-19, SNORD115-2, SNORD115-29, SNORD115-3, SNORD115-36, SNORD115-4, SNORD115-43, SNORD115-5, SNORD115-6, SNORD115-7, SNORD115-8, SNORD115-9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568550
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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