A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044011



Internal ID18786542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10507806..10542903hg38UCSC Ensembl
Innerchr11:10529353..10564450hg19UCSC Ensembl
Innerchr11:10485929..10521026hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3835098
hg1935098
hg1835098
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512688
Samples
Known GenesMIR4485, MRVI1-AS1, MTRNR2L8, RNF141
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044011
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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