A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6334676



Internal ID9373328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9988454..9997710hg38UCSC Ensembl
chr21:10466482..10475738hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg389257
hg199257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677510
Supporting Variants
SamplesNA18565
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6334676
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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