A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757979



Internal ID20533839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172787229..172787229hg38UCSC Ensembl
chr5:172214232..172214232hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289336
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757979
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