A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642319



Internal ID7029089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:41282857..41299868hg38UCSC Ensembl
Innerchr18:41282929..41299797hg38UCSC Ensembl
Outerchr18:41282786..41299940hg38UCSC Ensembl
chr18:38862821..38879832hg19UCSC Ensembl
Innerchr18:38862893..38879761hg19UCSC Ensembl
Outerchr18:38862750..38879904hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3817012
hg1917012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15851826
SamplesHG01796
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642319
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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