A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741987



Internal ID20517966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:26428329..26428747hg38UCSC Ensembl
chr5:26428438..26428856hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279257
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741987
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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