A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv831e199



Internal ID22758604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38340579..38342078hg38UCSC Ensembl
chr22:38736584..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 Variants
Supporting Variantsesv2661024, esv2671363
SamplesNA19397, NA19204, NA19332, NA19443, NA19107, NA19373, NA19131, NA20291, NA19137, NA20340, NA19238, NA19403, NA19152, NA18933, NA18516, NA18981, NA19469, NA19395, NA18858, NA19390, NA18909, NA19240, NA19144, NA19428, HG01108, NA19398, NA20348, NA19248, NA19093, NA19116, NA19711
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv831e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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