A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048183



Internal ID18790714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25053389..25083568hg38UCSC Ensembl
Innerchr15:25298536..25328715hg19UCSC Ensembl
Innerchr15:22849629..22879808hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3830180
hg1930180
hg1830180
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2474n100
Supporting Variantsnssv3545408
Samples
Known GenesSNORD116-10, SNORD116-11, SNORD116-12, SNORD116-13, SNORD116-14, SNORD116-15, SNORD116-16, SNORD116-2, SNORD116-3, SNORD116-4, 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)nsv1048183
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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