A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513026



Internal ID20886366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86655773..86750359hg38UCSC Ensembl
chr16:86689379..86783965hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3894587
hg1994587
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513026
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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