A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1096295



Internal ID1613118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73519906..73519980hg19UCSC Ensembl
chr10:73189912..73189986hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg1975
hg1875
Variant TypeCNV Deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv3779588
SamplesHuRef
Known GenesC10orf54, CDH23
Method
AnalysisRegion identical to calls - DGVa curated
PlatformSanger Sequencing
Comments
ReferenceLevy et al 2007
Pubmed ID17803354
Accession Number(s)esv1096295
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer