A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044878



Internal ID18787409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101482129..101919041hg38UCSC Ensembl
Innerchr15:102022334..102459244hg19UCSC Ensembl
Innerchr15:99839857..100276767hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38436913
hg19436911
hg18436911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2677n100
Supporting Variantsnssv3555350
Samples
Known GenesOR4F13P, OR4F15, OR4F6, PCSK6, TARSL2, TM2D3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044878
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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