A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996683



Internal ID21906026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1940891..1940947hg38UCSC Ensembl
chr4:1942618..1942674hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544514
Samples
Known GenesWHSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996683
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