A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046452



Internal ID19135671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:36439408..36481529hg38UCSC Ensembl
Innerchr11:36460958..36503079hg19UCSC Ensembl
Innerchr11:36417534..36459655hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3842122
hg1942122
hg1842122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512979
Samples
Known GenesPRR5L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046452
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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