A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3369397



Internal ID14869656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36463311..36463620hg38UCSC Ensembl
Innerchr18:36463310..36463621hg38UCSC Ensembl
Outerchr18:36463201..36463740hg38UCSC Ensembl
chr18:34043274..34043583hg19UCSC Ensembl
Innerchr18:34043273..34043584hg19UCSC Ensembl
Outerchr18:34043164..34043703hg19UCSC Ensembl
chr18:32297272..32297581hg18UCSC Ensembl
Innerchr18:32297582..32297271hg18UCSC Ensembl
Outerchr18:32297162..32297701hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38310
hg19310
hg18310
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8808812
SamplesNA12878
Known GenesFHOD3
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3369397
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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