A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624264



Internal ID6664431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94923968..95099386hg38UCSC Ensembl
chr10:96683725..96859143hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38175419
hg19175419
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13902138
SamplesHG03388
Known GenesCYP2C8, CYP2C9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624264
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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