A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678858



Internal ID9944963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9043819..9047336hg38UCSC Ensembl
Outerchr18:9043662..9047489hg38UCSC Ensembl
Innerchr18:9043817..9047334hg19UCSC Ensembl
Outerchr18:9043660..9047487hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg383828
hg193828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv581e199
Supporting Variantsessv5701358
SamplesNA20536
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678858
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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