A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039011



Internal ID19128230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5756780..5787897hg38UCSC Ensembl
Innerchr11:5778010..5809127hg19UCSC Ensembl
Innerchr11:5734586..5765703hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3831118
hg1931118
hg1831118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1044n100
Supporting Variantsnssv3506967
Samples
Known GenesOR52N1, OR52N5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039011
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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