A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4167295



Internal ID11103147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33355631..33355782hg38UCSC Ensembl
chr22:33751617..33751768hg19UCSC Ensembl
chr22:32081617..32081768hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38152
hg19152
hg18152
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1661802
Supporting Variants
SamplesHuRef
Known GenesLARGE
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4167295
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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