A curated catalogue of human genomic structural variation




Variant Details

Variant: esv344



Internal ID25892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170581751..171009919hg19UCSC Ensembl
chr6:170423676..170851844hg18UCSC Ensembl
chr6:170499383..170927551hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV CNV
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variants
Samples
Known GenesDLL1, FAM120B, MIR4644, PDCD2, PSMB1, TBP
Method
AnalysisVariant regions only detected by the WGTP experimentation.
PlatformAgilent
Comments
ReferenceRedon et al 2006
Pubmed ID17122850
Accession Number(s)esv344
Frequency
Sample Size271
Observed Gainn/a
Observed Lossn/a
Observed Complexn/a
Frequencyn/a


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