A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048455



Internal ID18790986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5588553..5634163hg38UCSC Ensembl
Innerchr11:5609783..5655393hg19UCSC Ensembl
Innerchr11:5566359..5611969hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3845611
hg1945611
hg1845611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3517124
Samples
Known GenesTRIM34, TRIM6, TRIM6-TRIM34
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048455
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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