A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1495e214



Internal ID20122918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98064172..98118302hg38UCSC Ensembl
chr9:100826454..100880584hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3854131
hg1954131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3621202, esv3621200
SamplesHG01767
Known GenesNANS, TRIM14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1495e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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