A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1648968



Internal ID1532762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73256582..73256702hg19UCSC Ensembl
chr10:72926588..72926708hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg19121
hg18121
Variant TypeCNV Deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv4268365
SamplesHuRef
Known GenesCDH23
Method
AnalysisRegion identical to calls - DGVa curated
PlatformSanger Sequencing
Comments
ReferenceLevy et al 2007
Pubmed ID17803354
Accession Number(s)esv1648968
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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