A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019978



Internal ID21929321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11283781..11283863hg38UCSC Ensembl
chr10:11325744..11325826hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590908
Samples
Known GenesCELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019978
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