A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497349



Internal ID20870555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60747389..60750000hg38UCSC Ensembl
chr16:60781293..60783904hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg382612
hg192612
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193834
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497349
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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