A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520892



Internal ID18472487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55297572..55380687hg38UCSC Ensembl
Innerchr11:55065048..55148163hg19UCSC Ensembl
Innerchr11:54821624..54904739hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3883116
hg1983116
hg1883116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050431
Supporting Variants
Samples
Known GenesOR4A15, OR4A16, TRIM51HP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3520892
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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