A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553765



Internal ID16341174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23759988..23811740hg38UCSC Ensembl
Innerchr11:23781534..23833286hg19UCSC Ensembl
Innerchr11:23738110..23789862hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3851753
hg1951753
hg1851753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1696n54
Supporting Variantsnssv768961
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553765
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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