A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035729



Internal ID21945072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60227591..60227645hg38UCSC Ensembl
chr16:60261495..60261549hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631124
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035729
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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