A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5886019



Internal ID9063509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:37589520..37589614hg38UCSC Ensembl
Outerchr21:37589193..37589890hg38UCSC Ensembl
Innerchr21:38961916..38961822hg19UCSC Ensembl
Outerchr21:38961495..38962192hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38698
hg19698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2663428
Supporting Variants
SamplesHG00708
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5886019
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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