A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv965e199



Internal ID22758738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102857840..102862466hg38UCSC Ensembl
chr4:103778997..103783623hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg384627
hg194627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2678375, esv2665471
SamplesNA20795, NA19782, HG00185, HG00253, NA20530, HG00259, NA12830, NA11843
Known GenesUBE2D3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv965e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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