A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046011



Internal ID19135230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20818293..22145275hg38UCSC Ensembl
Innerchr15:21023622..22433226hg19UCSC Ensembl
Innerchr15:19283673..19934590hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381326983
hg191409605
hg18650918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2332n100
Supporting Variantsnssv3541260
Samples
Known GenesCT60, CXADRP2, LOC646214, LOC727924, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046011
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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