A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553477



Internal ID16340886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10381992..10408451hg38UCSC Ensembl
Innerchr11:10403539..10429998hg19UCSC Ensembl
Innerchr11:10360115..10386574hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3826460
hg1926460
hg1826460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv767791
Samples
Known GenesCAND1.11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553477
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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