A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1002882



Internal ID6715016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:10654865..10660243hg38UCSC Ensembl
Outerchr19:10765541..10770919hg19UCSC Ensembl
Outerchr19:10626541..10631919hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385379
hg195379
hg185379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563928
SamplesHuRef
Known GenesILF3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1002882
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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