A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005798



Internal ID7070892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:28897529..28900353hg38UCSC Ensembl
Outerchr4:28899151..28901975hg19UCSC Ensembl
Outerchr4:28508249..28511073hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg383298
hg193298
hg183298
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563463
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005798
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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