A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1504476



Internal ID1357663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89188535..89188672hg19UCSC Ensembl
chr16:87716036..87716173hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg19138
hg18138
Variant TypeCNV Deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv4204969
SamplesHuRef
Known GenesACSF3
Method
AnalysisRegion identical to calls - DGVa curated
PlatformSanger Sequencing
Comments
ReferenceLevy et al 2007
Pubmed ID17803354
Accession Number(s)esv1504476
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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