A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046764



Internal ID18789295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5420996..5476387hg38UCSC Ensembl
Innerchr11:5442226..5497617hg19UCSC Ensembl
Innerchr11:5398802..5454193hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3855392
hg1955392
hg1855392
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1042n100
Supporting Variantsnssv3509226
Samples
Known GenesOR51B5, OR51I1, OR51I2, OR51Q1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046764
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