A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046406



Internal ID19135625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20992019hg38UCSC Ensembl
Innerchr15:20585976..21197348hg19UCSC Ensembl
Innerchr15:18845990..19462007hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38611297
hg19611373
hg18616018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2237n100
Supporting Variantsnssv3537276, nssv3537277, nssv3714654
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, 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)nsv1046406
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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