A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1468e214



Internal ID22757362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30419800..30568543hg38UCSC Ensembl
chr9:30419798..30568541hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38148744
hg19148744
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3620244, esv3620242
SamplesNA20278, NA20815
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1468e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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