A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044441



Internal ID19133660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25170021..25226010hg38UCSC Ensembl
Innerchr15:25415168..25471157hg19UCSC Ensembl
Innerchr15:22966261..23022250hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3855990
hg1955990
hg1855990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2482n100
Supporting Variantsnssv3545459, nssv3545458
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, SNORD115-36, 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)nsv1044441
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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