A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040586



Internal ID18783117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101785285..101880592hg38UCSC Ensembl
Innerchr15:102325488..102420795hg19UCSC Ensembl
Innerchr15:100143011..100238318hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3895308
hg1995308
hg1895308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555410
Samples
Known GenesOR4F13P, OR4F15, OR4F6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040586
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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