A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752203



Internal ID20528063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135742961..135742961hg38UCSC Ensembl
chr5:135078650..135078650hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752203
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