A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036326



Internal ID18778857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55591972..55679977hg38UCSC Ensembl
Innerchr11:55359448..55447453hg19UCSC Ensembl
Innerchr11:55116024..55204029hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3888006
hg1988006
hg1888006
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1176n100
Supporting Variantsnssv3512104, nssv3519699, nssv3511768, nssv3505538
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)nsv1036326
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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