A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514252



Internal ID20887604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34223182..34248819hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3825638
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514252
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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