A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045375



Internal ID18787906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55593873..55615262hg38UCSC Ensembl
Innerchr11:55361349..55382738hg19UCSC Ensembl
Innerchr11:55117925..55139314hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3821390
hg1921390
hg1821390
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508180
Samples
Known GenesOR4C11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045375
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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