A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038036



Internal ID18780567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55595852..55695666hg38UCSC Ensembl
Innerchr11:55363328..55463142hg19UCSC Ensembl
Innerchr11:55119904..55219718hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3899815
hg1999815
hg1899815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1179n100
Supporting Variantsnssv3504543
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)nsv1038036
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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