A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553597



Internal ID16341006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18075934..18078475hg38UCSC Ensembl
Innerchr11:18097481..18100022hg19UCSC Ensembl
Innerchr11:18054057..18056598hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382542
hg192542
hg182542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1668n54
Supporting Variantsnssv768339, nssv768338, nssv768340
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553597
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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