A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665892



Internal ID9585311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:61916711..61918438hg38UCSC Ensembl
Outerchr18:61916660..61918488hg38UCSC Ensembl
Innerchr18:59583944..59585671hg19UCSC Ensembl
Outerchr18:59583893..59585721hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg381829
hg191829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5969888, essv5992838
SamplesNA18530, NA19063
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665892
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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