A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066245



Internal ID21975478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139057282..139057282hg38UCSC Ensembl
chr5:138392971..138392971hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg382366
hg192366
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555451
Samples
Known GenesSIL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066245
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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