A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516446



Internal ID18814727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5583207..5599187hg38UCSC Ensembl
Innerchr11:5604437..5620417hg19UCSC Ensembl
Innerchr11:5561013..5576993hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3815981
hg1915981
hg1815981
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054035
Supporting Variants
Samples
Known GenesTRIM6, 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)nssv3516446
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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