A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554802



Internal ID15995525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55572353..55679951hg38UCSC Ensembl
Innerchr11:55339829..55447427hg19UCSC Ensembl
Innerchr11:55096405..55204003hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38107599
hg19107599
hg18107599
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1906n54
Supporting Variantsnssv1174644, nssv775162
Samples1780862071_A
Known GenesOR4C11, OR4C16, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554802
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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