A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053172



Internal ID19142391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55654851..55835981hg38UCSC Ensembl
Innerchr11:55422327..55603457hg19UCSC Ensembl
Innerchr11:55178903..55360033hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38181131
hg19181131
hg18181131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1204n100
Supporting Variantsnssv3512778, nssv3520914
Samples
Known GenesOR4C6, OR5D13, OR5D14, 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)nsv1053172
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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