A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3867021



Internal ID11548164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88954683..88954740hg38UCSC Ensembl
chr16:89021091..89021148hg19UCSC Ensembl
chr16:87548592..87548649hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3858
hg1958
hg1858
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1437918
Supporting Variants
SamplesHuRef
Known GenesCBFA2T3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3867021
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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