A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513153



Internal ID15505889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:101038537..101040071hg38UCSC Ensembl
Outerchr4:101959694..101961228hg19UCSC Ensembl
Outerchr4:102178717..102180251hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg381535
hg191535
hg181535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626648
Samples1
Known GenesPPP3CA
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513153
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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