A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1328032



Internal ID12144468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26772113..26773839hg38UCSC Ensembl
chr22:27168076..27169802hg19UCSC Ensembl
chr22:25498076..25499802hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg381727
hg191727
hg181727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4057203
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1328032
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer