A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554037



Internal ID16341446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38227656..38328058hg38UCSC Ensembl
Innerchr11:38249206..38349608hg19UCSC Ensembl
Innerchr11:38205782..38306184hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38100403
hg19100403
hg18100403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1750n54
Supporting Variantsnssv771106
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554037
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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