A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047155



Internal ID19136374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..22112595hg38UCSC Ensembl
Innerchr15:20284054..22400546hg19UCSC Ensembl
Innerchr15:18544068..19901910hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382033795
hg192116493
hg181357843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2181n100
Supporting Variantsnssv3716006, nssv3536634
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, 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)nsv1047155
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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