A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048634



Internal ID19137853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55654851..55835752hg38UCSC Ensembl
Innerchr11:55422327..55603228hg19UCSC Ensembl
Innerchr11:55178903..55359804hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38180902
hg19180902
hg18180902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1204n100
Supporting Variantsnssv3518311
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)nsv1048634
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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