A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4057203



Internal ID11357985
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1328032
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4057203
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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