A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043232



Internal ID19132451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133541517..133564530hg38UCSC Ensembl
Innerchr11:133411412..133434425hg19UCSC Ensembl
Innerchr11:132916622..132939635hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3823014
hg1923014
hg1823014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514916
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043232
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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