A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054770



Internal ID19143989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98906756..98954634hg38UCSC Ensembl
Innerchr11:98777486..98825364hg19UCSC Ensembl
Innerchr11:98282696..98330574hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3847879
hg1947879
hg1847879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521279
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)nsv1054770
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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