A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1138e214



Internal ID22757032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133798604..133819464hg38UCSC Ensembl
chr5:133134295..133155155hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3820861
hg1920861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3606833, esv3606830
SamplesNA19917, HG04047, NA19439
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1138e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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