A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1128844



Internal ID1606351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32555000..32555000hg19UCSC Ensembl
chr6:32662978..32662978hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg19686
hg18686
Variant TypeCNV Insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv3651264
SamplesHuRef
Known GenesHLA-DRB1
Method
AnalysisRegion identical to calls - DGVa curated
PlatformSanger Sequencing
Comments
ReferenceLevy et al 2007
Pubmed ID17803354
Accession Number(s)esv1128844
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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