A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998785



Internal ID7064538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99909957..99910760hg38UCSC Ensembl
Innerchr3:99628801..99629604hg19UCSC Ensembl
Innerchr3:101111491..101112294hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38804
hg19804
hg18804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586864
SamplesHuRef
Known GenesCMSS1, FILIP1L, MIR548G
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998785
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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