A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054262



Internal ID18796793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55262739..55379162hg38UCSC Ensembl
Innerchr11:55030215..55146638hg19UCSC Ensembl
Innerchr11:54786791..54903214hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38116424
hg19116424
hg18116424
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1168n100
Supporting Variantsnssv3712392
Samples
Known GenesOR4A15, OR4A16, TRIM48, TRIM51HP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054262
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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