A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3503903



Internal ID18455498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4638628..4650235hg38UCSC Ensembl
Innerchr11:4659858..4671465hg19UCSC Ensembl
Innerchr11:4616434..4628041hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811608
hg1911608
hg1811608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035551
Supporting Variants
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)nssv3503903
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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