A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039264



Internal ID19128483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..22145275hg38UCSC Ensembl
Innerchr15:20564575..22433226hg19UCSC Ensembl
Innerchr15:18824589..19934590hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381785954
hg191868652
hg181110002
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3537597
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)nsv1039264
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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