A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010625



Internal ID7074576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39894770..39895410hg38UCSC Ensembl
Innerchr19:40385410..40386050hg19UCSC Ensembl
Innerchr19:45077250..45077890hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38641
hg19641
hg18641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586146
SamplesHuRef
Known GenesFCGBP
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010625
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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