A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764675



Internal ID16058631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4785642..4888994hg38UCSC Ensembl
Innerchr11:4806872..4910224hg19UCSC Ensembl
Innerchr11:4763448..4866800hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38103353
hg19103353
hg18103353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553179
Supporting Variants
Samples
Known GenesOR51F2, OR51S1, OR51T1, OR52R1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764675
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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