A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553679



Internal ID16341088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:20214906..20254400hg38UCSC Ensembl
Innerchr11:20236452..20275946hg19UCSC Ensembl
Innerchr11:20193028..20232522hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3839495
hg1939495
hg1839495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175085
Samples1780862575_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553679
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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