A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1487e214



Internal ID22757381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78547199..78555379hg38UCSC Ensembl
chr9:81162115..81170295hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg388181
hg198181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3620798, esv3620799
SamplesNA18525, HG01798, HG01799
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1487e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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