A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553774



Internal ID16341183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23980429..24088370hg38UCSC Ensembl
Innerchr11:24001975..24109916hg19UCSC Ensembl
Innerchr11:23958551..24066492hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38107942
hg19107942
hg18107942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768973
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553774
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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