A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1433786



Internal ID12250222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88950457..88950525hg38UCSC Ensembl
chr16:89016865..89016933hg19UCSC Ensembl
chr16:87544366..87544434hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3869
hg1969
hg1869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3717749
SamplesHuRef
Known GenesCBFA2T3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1433786
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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