A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038717



Internal ID19127936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25062735..25092283hg38UCSC Ensembl
Innerchr15:25307882..25337430hg19UCSC Ensembl
Innerchr15:22858975..22888523hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3829549
hg1929549
hg1829549
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545447
Samples
Known GenesSNORD116-10, 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, SNORD116-3, 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)nsv1038717
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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