A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048385



Internal ID18790916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55591972..55667639hg38UCSC Ensembl
Innerchr11:55359448..55435115hg19UCSC Ensembl
Innerchr11:55116024..55191691hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3875668
hg1975668
hg1875668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1173n100
Supporting Variantsnssv3505073, nssv3509835, nssv3504221
Samples
Known GenesOR4C11, OR4C6, 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)nsv1048385
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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