A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553780



Internal ID16341189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24088370..24174573hg38UCSC Ensembl
Innerchr11:24109916..24196119hg19UCSC Ensembl
Innerchr11:24066492..24152695hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3886204
hg1986204
hg1886204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1700n54
Supporting Variantsnssv768976
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553780
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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