A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv107e180



Internal ID22757517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52993109..53007503hg38UCSC Ensembl
chr3:53027125..53041519hg19UCSC Ensembl
chr3:53002165..53016559hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3814395
hg1914395
hg1814395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv996791, esv991487, esv1009936, esv993207
SamplesHuRef
Known GenesSFMBT1
MethodOligo aCGH
SNP array
AnalysisPooled samples.
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)dgv107e180
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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