A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497243



Internal ID20870448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61023780..61025484hg38UCSC Ensembl
chr16:61057684..61059388hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381705
hg191705
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190954
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497243
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