A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504289



Internal ID20877550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68635261..68641971hg38UCSC Ensembl
chr16:68669164..68675874hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg386711
hg196711
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504289
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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