A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039182



Internal ID19128401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25170021..25210965hg38UCSC Ensembl
Innerchr15:25415168..25456112hg19UCSC Ensembl
Innerchr15:22966261..23007205hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3840945
hg1940945
hg1840945
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2481n100
Supporting Variantsnssv3545454
Samples
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, SNORD115-20, SNORD115-21, SNORD115-22, SNORD115-29, SNORD115-3, SNORD115-36, SNORD115-4, SNORD115-43, SNORD115-5, SNORD115-6, SNORD115-7, SNORD115-8, SNORD115-9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039182
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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