A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044243



Internal ID19133462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5379806..5411086hg38UCSC Ensembl
Innerchr11:5401036..5432316hg19UCSC Ensembl
Innerchr11:5357612..5388892hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3831281
hg1931281
hg1831281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514027
Samples
Known GenesOR51B5, OR51M1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044243
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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