A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044303



Internal ID19133522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7808373..7877006hg38UCSC Ensembl
Innerchr11:7829920..7898553hg19UCSC Ensembl
Innerchr11:7786496..7855129hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3868634
hg1968634
hg1868634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514087
Samples
Known GenesLOC283299, OR5E1P, OR5P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044303
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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