A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046131



Internal ID19135350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20364686..22233250hg38UCSC Ensembl
Innerchr15:20569939..22521201hg19UCSC Ensembl
Innerchr15:18829953..20022565hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381868565
hg191951263
hg181192613
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3713805
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, 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)nsv1046131
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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