A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511485



Internal ID15504224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55598285..55660224hg38UCSC Ensembl
Outerchr11:55595479..55662691hg38UCSC Ensembl
Innerchr11:55365761..55427700hg19UCSC Ensembl
Outerchr11:55362955..55430167hg19UCSC Ensembl
Innerchr11:55122337..55184276hg18UCSC Ensembl
Outerchr11:55119531..55186743hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3867213
hg1967213
hg1867213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626102
Samples1
Known GenesOR4C11, OR4P4, OR4S2
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511485
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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