A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1173419



Internal ID11989856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33673860..33673981hg38UCSC Ensembl
chr22:34069846..34069967hg19UCSC Ensembl
chr22:32399846..32399967hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38122
hg19122
hg18122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3782813
SamplesHuRef
Known GenesLARGE
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1173419
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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