A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642219



Internal ID6682300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36224889..36230256hg38UCSC Ensembl
chr18:33804852..33810219hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg385368
hg195368
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15842423, essv15842424, essv15842422
SamplesHG00189, NA12273, NA12272
Known GenesMOCOS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642219
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer