A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509959



Internal ID18461554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55701036..56242711hg38UCSC Ensembl
Innerchr11:55468512..56010187hg19UCSC Ensembl
Innerchr11:55225088..55766763hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38541676
hg19541676
hg18541676
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043441
Supporting Variants
Samples
Known GenesOR10AG1, OR5AS1, OR5D13, OR5D14, OR5D16, OR5D18, OR5F1, OR5I1, OR5J2, OR5L1, OR5L2, OR5T2, OR5W2, OR7E5P, OR8H2, OR8H3, OR8I2, OR8J3, OR8K5, TRIM51
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3509959
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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