A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1908e1



Internal ID6309706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29469101..29672665hg19UCSC Ensembl
chr6:29577080..29780644hg18UCSC Ensembl
chr6:29577080..29780644hg17UCSC Ensembl
Cytoband6p22.1
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 Variantsessv10262, esv171
SamplesNA18506
Known GenesGABBR1, LOC100507362, MOG, OR2H2, SNORD32B, UBD, ZFP57
Method
Analysis
Platform
Comments
ReferenceRedon et al 2006
Pubmed ID17122850
Accession Number(s)dgv1908e1
Frequency
Sample Size271
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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