A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13902087



Internal ID3903903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94644907..94724573hg38UCSC Ensembl
chr10:96404664..96484330hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3879667
hg1979667
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624254
Supporting Variants
SamplesHG00690
Known GenesCYP2C18
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13902087
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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