A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1238e214



Internal ID22757132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164326941..164408560hg38UCSC Ensembl
chr6:164747974..164829593hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3881620
hg1981620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3611594, esv3611595
SamplesHG00187, NA19089
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1238e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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