A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1493e214



Internal ID20122916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94545750..94588367hg38UCSC Ensembl
chr9:97308032..97350649hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3842618
hg1942618
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3621130, esv3621132
SamplesHG04229
Known GenesFBP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1493e214
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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