A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624254



Internal ID6664421
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13902087, essv13902086, essv13902088
SamplesHG00185, HG00690, HG01866
Known GenesCYP2C18
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624254
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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