A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042501



Internal ID19131720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5829641..5866695hg38UCSC Ensembl
Innerchr11:5850871..5887925hg19UCSC Ensembl
Innerchr11:5807447..5844501hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3837055
hg1937055
hg1837055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1053n100
Supporting Variantsnssv3506794
Samples
Known GenesOR52E6, OR52E8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042501
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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