A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049089



Internal ID18791620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12170114..12183719hg38UCSC Ensembl
Innerchr11:12191661..12205266hg19UCSC Ensembl
Innerchr11:12148237..12161842hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3813606
hg1913606
hg1813606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519879
Samples
Known GenesMICAL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049089
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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