A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498449



Internal ID20871659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12524845..12530842hg38UCSC Ensembl
chr16:12618702..12624699hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg385998
hg195998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193486
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498449
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer