A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513041



Internal ID15852463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:32765172..32766634hg38UCSC Ensembl
Outerchr3:32806664..32808126hg19UCSC Ensembl
Outerchr3:32781668..32783130hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381463
hg191463
hg181463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626524
Samples1
Known GenesCNOT10
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513041
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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