A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036447



Internal ID19125666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..22100273hg38UCSC Ensembl
Innerchr15:20585976..22388224hg19UCSC Ensembl
Innerchr15:18845990..19889588hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381719551
hg191802249
hg181043599
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2250n100
Supporting Variantsnssv3537363, nssv3714673, nssv3537365, nssv3537364
Samples
Known GenesCT60, 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)nsv1036447
Frequency
Sample Size11257
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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