A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626769



Internal ID15850302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:133583088..133589469hg38UCSC Ensembl
Outerchr5:132918779..132925160hg19UCSC Ensembl
Outerchr5:132946678..132953059hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg386382
hg196382
hg186382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513262
Supporting Variants
Samples1
Known GenesFSTL4
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626769
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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