A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641751



Internal ID7028522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9690516..9696576hg38UCSC Ensembl
chr18:9690513..9696573hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg386061
hg196061
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15802936, essv15802935, essv15802934, essv15802933
SamplesNA19379, NA18916, HG02884, HG04134
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641751
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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