A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1655e1



Internal ID6309453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103780705..103942445hg19UCSC Ensembl
chr4:103999805..104161894hg18UCSC Ensembl
chr4:104137960..104300049hg17UCSC Ensembl
Cytoband4q24
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 Variantsessv3884, essv22104, essv12179, essv24673, essv10866
SamplesNA18871, NA18994, NA10857, NA19101, NA11829
Known GenesCISD2, SLC9B1, UBE2D3
Method
Analysis
Platform
Comments
ReferenceRedon et al 2006
Pubmed ID17122850
Accession Number(s)dgv1655e1
Frequency
Sample Size271
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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