A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587193



Internal ID6711889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35132335..35132910hg38UCSC Ensembl
Innerchr19:35623239..35623814hg19UCSC Ensembl
Innerchr19:40315079..40315654hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38576
hg19576
hg18576
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv993226
Supporting Variants
SamplesHuRef
Known GenesLGI4
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587193
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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