A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766711



Internal ID20542571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32208596..32208596hg38UCSC Ensembl
chr5:32208702..32208702hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288276
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766711
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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