A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513136



Internal ID15852558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:65774191..65777949hg38UCSC Ensembl
Outerchr4:66639909..66643667hg19UCSC Ensembl
Outerchr4:66322504..66326262hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg383759
hg193759
hg183759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626629
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)nsv513136
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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