A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555096



Internal ID15995819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56316968..56467585hg38UCSC Ensembl
Innerchr11:56084444..56235061hg19UCSC Ensembl
Innerchr11:55841020..55991637hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38150618
hg19150618
hg18150618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1948n54
Supporting Variantsnssv776858
Samples
Known GenesOR5M9, OR5R1, OR8J1, OR8K1, OR8K3, OR8U1, OR8U8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555096
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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