A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029469



Internal ID21938812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57533693..57533749hg38UCSC Ensembl
chr16:57567605..57567661hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620691
Samples
Known GenesCCDC102A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029469
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