A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508645



Internal ID20881949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59870439..60012149hg38UCSC Ensembl
chr16:59904343..60046053hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38141711
hg19141711
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177942
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508645
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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