A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049004



Internal ID18791535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55693312..56247291hg38UCSC Ensembl
Innerchr11:55460788..56014767hg19UCSC Ensembl
Innerchr11:55217364..55771343hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38553980
hg19553980
hg18553980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1205n100
Supporting Variantsnssv3519797
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)nsv1049004
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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