A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999697



Internal ID21909040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43983061..43989955hg38UCSC Ensembl
chr5:43983163..43990057hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg386895
hg196895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549199
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999697
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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