A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037096



Internal ID19126315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56565274..56613443hg38UCSC Ensembl
Innerchr11:56332750..56380919hg19UCSC Ensembl
Innerchr11:56089326..56137495hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3848170
hg1948170
hg1848170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504685
Samples
Known GenesOR5M1, OR5M10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037096
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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