A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511513



Internal ID20884841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9670580..9676964hg38UCSC Ensembl
chr16:9764437..9770821hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg386385
hg196385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179674
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511513
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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