A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998756



Internal ID7081932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:38968576..38975766hg38UCSC Ensembl
Outerchr22:39364581..39371771hg19UCSC Ensembl
Outerchr22:37694527..37701717hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg387191
hg197191
hg187191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563651
SamplesHuRef
Known GenesAPOBEC3A_B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998756
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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