A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505883



Internal ID20879157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88918932..89020305hg38UCSC Ensembl
chr16:88985340..89086713hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38101374
hg19101374
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180902
Samples
Known GenesCBFA2T3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505883
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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