A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035675



Internal ID19124894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7756059..7848361hg38UCSC Ensembl
Innerchr11:7777606..7869908hg19UCSC Ensembl
Innerchr11:7734182..7826484hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3892303
hg1992303
hg1892303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504037
Samples
Known GenesOR5P2, OR5P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035675
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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