A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042841



Internal ID19132060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55654851..55844339hg38UCSC Ensembl
Innerchr11:55422327..55611815hg19UCSC Ensembl
Innerchr11:55178903..55368391hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38189489
hg19189489
hg18189489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1204n100
Supporting Variantsnssv3512618
Samples
Known GenesOR4C6, OR5D13, OR5D14, OR5D16, OR5D18, OR5L1, OR5L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042841
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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