A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1492e214



Internal ID22757386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94486938..94547326hg38UCSC Ensembl
chr9:97249220..97309608hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3860389
hg1960389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3621125, esv3621127
SamplesNA18626
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1492e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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