A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556442



Internal ID15997165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:112994393..113041326hg38UCSC Ensembl
Innerchr11:112865115..112912048hg19UCSC Ensembl
Innerchr11:112370325..112417258hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3846934
hg1946934
hg1846934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784579
Samples
Known GenesNCAM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556442
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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