A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1092896



Internal ID1442634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13231429..13231558hg19UCSC Ensembl
chr6:13339408..13339537hg18UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg19130
hg18130
Variant TypeCNV Deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv4294223
SamplesHuRef
Known GenesPHACTR1
Method
AnalysisRegion identical to calls - DGVa curated
PlatformSanger Sequencing
Comments
ReferenceLevy et al 2007
Pubmed ID17803354
Accession Number(s)esv1092896
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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