A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2024e1



Internal ID6309822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160372244..161234665hg19UCSC Ensembl
chr6:160292234..161154655hg18UCSC Ensembl
chr6:160342655..161205076hg17UCSC Ensembl
Cytoband6q25.3
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 Variantsesv738, essv2852, essv3847
SamplesNA18953
Known GenesIGF2R, LOC729603, LPA, LPAL2, PLG, SLC22A1, SLC22A2, SLC22A3
Method
Analysis
Platform
Comments
ReferenceRedon et al 2006
Pubmed ID17122850
Accession Number(s)dgv2024e1
Frequency
Sample Size271
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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