A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403686



Internal ID22461556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42349415..42349620hg38UCSC Ensembl
chr21:43769524..43769729hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966889
Supporting Variants
Samples
Known GenesTFF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403686
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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