A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661024



Internal ID9927129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38340736..38341925hg38UCSC Ensembl
Outerchr22:38340579..38342078hg38UCSC Ensembl
Innerchr22:38736741..38737930hg19UCSC Ensembl
Outerchr22:38736584..38738083hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv831e199
Supporting Variantsessv5402515, essv6453561, essv5811414, essv5763593, essv6004861, essv5791933, essv5549205, essv6514261, essv5462379, essv6312668, essv5609312, essv5782873, essv5640491, essv6348314, essv5654962, essv6588482, essv5856782, essv5461459, essv5722397, essv5410266
SamplesNA19397, NA19332, NA19443, NA19107, NA19373, NA20291, NA20340, NA19403, NA18933, NA18516, NA19469, NA19395, NA19390, NA19428, HG01108, NA19398, NA20348, NA19248, NA19093, NA19711
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661024
Frequency
Sample Size1151
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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