A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1494e214



Internal ID20122917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97595020..97658603hg38UCSC Ensembl
chr9:100357302..100420885hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3863584
hg1963584
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3621193, esv3621192
SamplesHG04152, HG01602
Known GenesNCBP1, TMOD1, TSTD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1494e214
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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