A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563928



Internal ID6688311
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1002882
Supporting Variants
SamplesHuRef
Known GenesILF3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563928
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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