A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510447



Internal ID20883765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63000111..63031952hg38UCSC Ensembl
chr16:63034015..63065856hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3831842
hg1931842
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510447
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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