A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3540851



Internal ID18839132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20406104..22279197hg38UCSC Ensembl
Innerchr15:20611357..22567148hg19UCSC Ensembl
Innerchr15:18871371..20068512hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381873094
hg191955792
hg181197142
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046569
Supporting Variants
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3540851
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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