A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060926



Internal ID18803457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3093486..3319621hg38UCSC Ensembl
Innerchr17:2996780..3222915hg19UCSC Ensembl
Innerchr17:2943530..3169665hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38226136
hg19226136
hg18226136
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560089
Samples
Known GenesOR1A1, OR1A2, OR1D4, OR1G1, OR3A1, OR3A2, OR3A4P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060926
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer