A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553766



Internal ID16341175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23759988..23819629hg38UCSC Ensembl
Innerchr11:23781534..23841175hg19UCSC Ensembl
Innerchr11:23738110..23797751hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3859642
hg1959642
hg1859642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1696n54
Supporting Variantsnssv768962, nssv768963
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553766
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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