A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1455e214



Internal ID22757349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16058917..16098796hg38UCSC Ensembl
chr9:16058915..16098794hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3839880
hg1939880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3619804, esv3619806
SamplesNA19355, HG02070, NA18981, NA19434
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1455e214
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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