A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5684311



Internal ID8661714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:31423315..31424204hg38UCSC Ensembl
Outerchr18:31423278..31424254hg38UCSC Ensembl
Innerchr18:29003278..29004167hg19UCSC Ensembl
Outerchr18:29003241..29004217hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38977
hg19977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661620
Supporting Variants
SamplesNA18907
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5684311
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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