A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641829



Internal ID7028600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12187417..12201616hg38UCSC Ensembl
chr18:12187416..12201615hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3814200
hg1914200
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15811014, essv15811012, essv15811011, essv15811013
SamplesHG02811, NA19108, HG03681, HG03313
Known GenesC18orf61
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641829
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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