A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039236



Internal ID18781767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55595852..55685521hg38UCSC Ensembl
Innerchr11:55363328..55452997hg19UCSC Ensembl
Innerchr11:55119904..55209573hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3889670
hg1989670
hg1889670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1179n100
Supporting Variantsnssv3517104, nssv3517693, nssv3520039, nssv3522124
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)nsv1039236
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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