A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1348586



Internal ID1046496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50830086..50830086hg19UCSC Ensembl
chr10:50500092..50500092hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg19132
hg18132
Variant TypeCNV Insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv4059620
SamplesHuRef
Known GenesCHAT
Method
AnalysisRegion identical to calls - DGVa curated
PlatformSanger Sequencing
Comments
ReferenceLevy et al 2007
Pubmed ID17803354
Accession Number(s)esv1348586
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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