A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513155



Internal ID15852577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:102408134..102411668hg38UCSC Ensembl
Outerchr4:103329291..103332825hg19UCSC Ensembl
Outerchr4:103548314..103551848hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg383535
hg193535
hg183535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626650
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513155
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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