A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560086



Internal ID18511681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3045742..3209683hg38UCSC Ensembl
Innerchr17:2949036..3112977hg19UCSC Ensembl
Innerchr17:2895786..3059727hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38163942
hg19163942
hg18163942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060727
Supporting Variants
Samples
Known GenesOR1A2, OR1D2, OR1D5, OR1G1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560086
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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