A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13902093



Internal ID3903909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94735462..94815612hg38UCSC Ensembl
chr10:96495219..96575369hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3880151
hg1980151
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624257
Supporting Variants
SamplesHG00268
Known GenesCYP2C18, CYP2C19
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13902093
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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