A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052960



Internal ID19142179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98956616..99008406hg38UCSC Ensembl
Innerchr11:98827346..98879136hg19UCSC Ensembl
Innerchr11:98332556..98384346hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3851791
hg1951791
hg1851791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521358
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)nsv1052960
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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