A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554036



Internal ID16341445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38227656..38318734hg38UCSC Ensembl
Innerchr11:38249206..38340284hg19UCSC Ensembl
Innerchr11:38205782..38296860hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3891079
hg1991079
hg1891079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1750n54
Supporting Variantsnssv1174627, nssv771104, nssv771105
Samples1782681169_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554036
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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