A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053297



Internal ID18795828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4637957..4649391hg38UCSC Ensembl
Innerchr11:4659187..4670621hg19UCSC Ensembl
Innerchr11:4615763..4627197hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811435
hg1911435
hg1811435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1025n100
Supporting Variantsnssv3522307
Samples
Known GenesOR51D1, OR51E1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053297
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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