A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036880



Internal ID19126099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376186..20996195hg38UCSC Ensembl
Innerchr15:20581439..21201524hg19UCSC Ensembl
Innerchr15:18841453..19466183hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38620010
hg19620086
hg18624731
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2237n100
Supporting Variantsnssv3535903, nssv3535902
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, 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)nsv1036880
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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