A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999867



Internal ID21909210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:37708979..37719526hg38UCSC Ensembl
chr5:37709081..37719628hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3810548
hg1910548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553875
Samples
Known GenesWDR70
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999867
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