A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514721



Internal ID20888076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28210801..28212400hg38UCSC Ensembl
chr16:28222122..28223721hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190904
Samples
Known GenesXPO6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514721
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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