A curated catalogue of human genomic structural variation




Variant Details

Variant: esv989898



Internal ID7061141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133583276..133589301hg38UCSC Ensembl
chr5:132918967..132924992hg19UCSC Ensembl
chr5:132946866..132952891hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg386026
hg196026
hg186026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv151e180
Supporting Variantsessv3570611
SamplesHuRef
Known GenesFSTL4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv989898
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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