A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507957



Internal ID20881254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88963950..89121712hg38UCSC Ensembl
chr16:89030358..89188120hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38157763
hg19157763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180013
Samples
Known GenesACSF3, CBFA2T3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507957
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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