A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005153



Internal ID6717276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:93816149..93817806hg38UCSC Ensembl
Outerchr1:94281705..94283362hg19UCSC Ensembl
Outerchr1:94054293..94055950hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381658
hg191658
hg181658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565354
SamplesHuRef
Known GenesBCAR3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005153
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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