A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667264



Internal ID9933369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:37946247..37948591hg38UCSC Ensembl
Outerchr22:37946213..37948626hg38UCSC Ensembl
Innerchr22:38342254..38344598hg19UCSC Ensembl
Outerchr22:38342220..38344633hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg382414
hg192414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv830e199
Supporting Variantsessv6441262
SamplesNA19462
Known GenesC22orf23
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667264
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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