A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046244



Internal ID18788775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25170021..25252158hg38UCSC Ensembl
Innerchr15:25415168..25497305hg19UCSC Ensembl
Innerchr15:22966261..23048398hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3882138
hg1982138
hg1882138
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2479n100
Supporting Variantsnssv3545491, nssv3545494, nssv3545495, nssv3545488, nssv3545497, nssv3545489, nssv3545493, nssv3545496, nssv3545492, nssv3545490
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, SNORD115-33, SNORD115-34, SNORD115-35, SNORD115-36, SNORD115-37, SNORD115-38, SNORD115-39, SNORD115-4, SNORD115-40, SNORD115-41, SNORD115-42, SNORD115-43, SNORD115-44, 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)nsv1046244
Frequency
Sample Size29084
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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