A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051341



Internal ID19140560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25170021..25230658hg38UCSC Ensembl
Innerchr15:25415168..25475805hg19UCSC Ensembl
Innerchr15:22966261..23026898hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3860638
hg1960638
hg1860638
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2482n100
Supporting Variantsnssv3545461
Samples
Known GenesPWAR4, SNORD115-1, 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, SNORD115-23, SNORD115-24, SNORD115-25, SNORD115-26, SNORD115-27, SNORD115-28, SNORD115-29, SNORD115-3, SNORD115-30, SNORD115-31, SNORD115-32, 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)nsv1051341
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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