A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1089089



Internal ID11905527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132191967..132192076hg38UCSC Ensembl
chr10:134005471..134005580hg19UCSC Ensembl
chr10:133855461..133855570hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38110
hg19110
hg18110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4320925
SamplesHuRef
Known GenesDPYSL4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1089089
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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