A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999299



Internal ID7082134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:158630671..158640368hg38UCSC Ensembl
Outerchr3:158348460..158358157hg19UCSC Ensembl
Outerchr3:159831154..159840851hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg389698
hg199698
hg189698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565517
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999299
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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