A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647789



Internal ID7034528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41085183..41087107hg38UCSC Ensembl
Innerchr22:41085233..41087057hg38UCSC Ensembl
Outerchr22:41085118..41087172hg38UCSC Ensembl
chr22:41481187..41483111hg19UCSC Ensembl
Innerchr22:41481237..41483061hg19UCSC Ensembl
Outerchr22:41481122..41483176hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg381925
hg191925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16430097
SamplesNA20522
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647789
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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