A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998147



Internal ID7081550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:30165808..30174299hg38UCSC Ensembl
Outerchr19:30656715..30665206hg19UCSC Ensembl
Outerchr19:35348555..35357046hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg388492
hg198492
hg188492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565100
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998147
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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