A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051928



Internal ID18794459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55591972..55661919hg38UCSC Ensembl
Innerchr11:55359448..55429395hg19UCSC Ensembl
Innerchr11:55116024..55185971hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3869948
hg1969948
hg1869948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1173n100
Supporting Variantsnssv3521875
Samples
Known GenesOR4C11, OR4P4, OR4S2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051928
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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