A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5618619



Internal ID8966432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:23541007..23548332hg38UCSC Ensembl
Outerchr1:23540850..23548520hg38UCSC Ensembl
Innerchr1:23867498..23874823hg19UCSC Ensembl
Outerchr1:23867341..23875011hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg387671
hg197671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659031
Supporting Variants
SamplesHG00536
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5618619
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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