A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553596



Internal ID16341005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18075934..18078216hg38UCSC Ensembl
Innerchr11:18097481..18099763hg19UCSC Ensembl
Innerchr11:18054057..18056339hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382283
hg192283
hg182283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1668n54
Supporting Variantsnssv768337
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553596
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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