A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586850



Internal ID6711546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15159976..15160424hg38UCSC Ensembl
Innerchr19:15270787..15271235hg19UCSC Ensembl
Innerchr19:15131787..15132235hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38449
hg19449
hg18449
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv997404
Supporting Variants
SamplesHuRef
Known GenesNOTCH3
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586850
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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