A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5675957



Internal ID8653360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38528422..38528746hg38UCSC Ensembl
chr21:39900346..39900670hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672087
Supporting Variants
SamplesNA18853
Known GenesERG
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5675957
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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