A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553795



Internal ID16341204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24419419..24430480hg38UCSC Ensembl
Innerchr11:24440965..24452026hg19UCSC Ensembl
Innerchr11:24397541..24408602hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3811062
hg1911062
hg1811062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1704n54
Supporting Variantsnssv768991, nssv768990
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553795
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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