A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv976e199



Internal ID22758749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:137615636..137619495hg38UCSC Ensembl
chr4:138536790..138540649hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg383860
hg193860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2674470, esv2665631
SamplesNA19704, NA19819, HG00106
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv976e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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