A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677800



Internal ID9943905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35438171..35438667hg38UCSC Ensembl
Outerchr22:35438134..35438717hg38UCSC Ensembl
Innerchr22:35834164..35834660hg19UCSC Ensembl
Outerchr22:35834127..35834710hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5898364, essv6039281
SamplesHG00536, NA18613
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677800
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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