A curated catalogue of human genomic structural variation




Variant Details

Variant: esv996135



Internal ID6732079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26772109..26773834hg38UCSC Ensembl
chr22:27168072..27169797hg19UCSC Ensembl
chr22:25498072..25499797hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg381726
hg191726
hg181726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3581893
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv996135
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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