A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054517



Internal ID18797048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101737277..101919041hg38UCSC Ensembl
Innerchr15:102277480..102459244hg19UCSC Ensembl
Innerchr15:100095003..100276767hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38181765
hg19181765
hg18181765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555407
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)nsv1054517
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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