A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2041e1



Internal ID6309839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170821217..171009919hg19UCSC Ensembl
chr6:170663142..170851844hg18UCSC Ensembl
chr6:170738849..170927551hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Complex
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv14781, essv4707
SamplesNA18622, NA19159
Known GenesPDCD2, PSMB1, TBP
Method
Analysis
Platform
Comments
ReferenceRedon et al 2006
Pubmed ID17122850
Accession Number(s)dgv2041e1
Frequency
Sample Size271
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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