A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043733



Internal ID19132952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20367351..22168141hg38UCSC Ensembl
Innerchr15:20572604..22456092hg19UCSC Ensembl
Innerchr15:18832618..19957456hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381800791
hg191883489
hg181124839
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3535818, nssv3535819
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)nsv1043733
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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