A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051795



Internal ID19141014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25170021..25228106hg38UCSC Ensembl
Innerchr15:25415168..25473253hg19UCSC Ensembl
Innerchr15:22966261..23024346hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3858086
hg1958086
hg1858086
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2482n100
Supporting Variantsnssv3545460
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, SNORD115-36, 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)nsv1051795
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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