A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990966



Internal ID7061627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:170147858..170158496hg38UCSC Ensembl
Outerchr4:171069009..171079647hg19UCSC Ensembl
Outerchr4:171305584..171316222hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3810639
hg1910639
hg1810639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563521
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990966
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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