A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642654



Internal ID7029423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58837959..58848849hg38UCSC Ensembl
chr18:56505191..56516081hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3810891
hg1910891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15894282, essv15894281
SamplesHG03740, HG03695
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642654
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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