A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670964



Internal ID9937069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38978115..38979725hg38UCSC Ensembl
Outerchr22:38978078..38979775hg38UCSC Ensembl
Innerchr22:39374120..39375730hg19UCSC Ensembl
Outerchr22:39374083..39375780hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381698
hg191698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6458186, essv5541844
SamplesNA07357, HG01198
Known GenesAPOBEC3A_B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670964
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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