A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038959



Internal ID19128178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20406104..22283866hg38UCSC Ensembl
Innerchr15:20611357..22571817hg19UCSC Ensembl
Innerchr15:18871371..20073181hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381877763
hg191960461
hg181201811
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3540852
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)nsv1038959
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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