A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1499e214



Internal ID22757393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104974916..104992894hg38UCSC Ensembl
chr9:107737197..107755175hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3817979
hg1917979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3621348, esv3621349
SamplesHG01506, HG03681, HG03698
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1499e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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