A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1189776



Internal ID1064070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107410626..107410711hg19UCSC Ensembl
chr7:107197862..107197947hg18UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg1986
hg1886
Variant TypeCNV Deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv4313862
SamplesHuRef
Known GenesSLC26A3
Method
AnalysisRegion identical to calls - DGVa curated
PlatformSanger Sequencing
Comments
ReferenceLevy et al 2007
Pubmed ID17803354
Accession Number(s)esv1189776
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