A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555406



Internal ID18507001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101685840..101919041hg38UCSC Ensembl
Innerchr15:102226043..102459244hg19UCSC Ensembl
Innerchr15:100043566..100276767hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38233202
hg19233202
hg18233202
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041586
Supporting Variants
Samples
Known GenesOR4F13P, OR4F15, OR4F6, TARSL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3555406
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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