A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504037



Internal ID18802318
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 StatusS
Merged Variantsnsv1035675
Supporting Variants
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)nssv3504037
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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