A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5760351



Internal ID9019632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:25898819..25925439hg38UCSC Ensembl
Outerchr18:25898757..25925504hg38UCSC Ensembl
Innerchr18:23478783..23505403hg19UCSC Ensembl
Outerchr18:23478721..23505468hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3826748
hg1926748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672989
Supporting Variants
SamplesHG00637
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5760351
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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