A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6009603



Internal ID9706399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23122555..23122995hg38UCSC Ensembl
chr20:23103192..23103632hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672564
Supporting Variants
SamplesNA19457
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6009603
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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