A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038331



Internal ID19127550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5762440..5787897hg38UCSC Ensembl
Innerchr11:5783670..5809127hg19UCSC Ensembl
Innerchr11:5740246..5765703hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3825458
hg1925458
hg1825458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1044n100
Supporting Variantsnssv3503231, nssv3513884, nssv3520385
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)nsv1038331
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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