A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678773



Internal ID9944878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:54561657..54566651hg38UCSC Ensembl
Outerchr18:54561620..54566701hg38UCSC Ensembl
Innerchr18:52228888..52233882hg19UCSC Ensembl
Outerchr18:52228851..52233932hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg385082
hg195082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6010155
SamplesHG00634
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678773
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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