A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641503



Internal ID6681588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:640491..689131hg38UCSC Ensembl
chr18:640491..689131hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3848641
hg1948641
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15772464, essv15772465
SamplesNA20896, NA20809
Known GenesC18orf56, CLUL1, ENOSF1, TYMS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641503
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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