A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565068



Internal ID7036168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:13573780..13582289hg38UCSC Ensembl
Outerchr3:13615280..13623789hg19UCSC Ensembl
Outerchr3:13590281..13598790hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg388510
hg198510
hg188510
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1004545
Supporting Variants
SamplesHuRef
Known GenesFBLN2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565068
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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