A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1446888



Internal ID12263325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88967168..88967168hg38UCSC Ensembl
chr16:89033576..89033576hg19UCSC Ensembl
chr16:87561077..87561077hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3854
hg1954
hg1854
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587546
SamplesHuRef
Known GenesCBFA2T3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1446888
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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